Therapeutic combinations comprising anti-cd73 antibodies and uses thereof

ABSTRACT

The present invention provides therapeutic combinations featuring anti-CD73 antibodies (e.g., MEDI9447) and A2A receptor inhibitors and methods of using such combinations for reducing tumor-mediated immunosuppression.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims benefit under 35 U.S.C. §119(e) of U.S.Provisional Application No. 62/078,243, filed Nov. 11, 2014, which isincorporated by reference herein in its entirety for all purposes.

SEQUENCE LISTING

The instant application contains a Sequence Listing which has beensubmitted electronically in ASCII format and is hereby incorporated byreference in its entirety. Said ASCII copy, created on Nov. 9, 2015, isnamed CD73-200US1_SL.txt and is 128,702 bytes in size.

BACKGROUND OF THE INVENTION

CD73 or ecto-5′nucleotidase (5′-NT) is ubiquitously expressed in anumber of tissues. This protein is anchored to the cell membrane througha glycosylphosphatidylinositol (GPI) linkage, has ecto-enzyme activity,and plays a role in signal transduction. The primary function of CD73 isthe conversion of extracellular nucleotides (e.g., 5′-AMP), to whichcells are generally impermeable, to their corresponding nucleosides(e.g., adenosine), which can readily enter most cells. CD73 productionof adenosine by the dephosphorylation of AMP, has been shown to regulateadenosine receptor engagement in many tissues, indicating that adenosinefunctions in cytoprotection, cell growth, angiogenesis andimmunosuppression, and also plays a role in tumorigenesis.

CD73 expression on tumor cells has been reported in several types ofcancer, including bladder cancer, leukemia, glioma, glioblastoma,melanoma, ovarian cancer, thyroid cancer, esophageal cancer, prostatecancer, and breast cancer. Elevated CD73 expression has also beenassociated with tumor invasiveness, metastasis, and reduced patientsurvival time. CD73 generates an immunosuppressed environment,characterized by increased adenosine levels, which promote thedevelopment and progression of cancer. Notably, CD73 expression has beenassociated with a prometastatic phenotype in melanoma and breast cancer.

Immune-checkpoint inhibitors hold great potential as cancertherapeutics. Nevertheless, clinical benefits from immune-checkpointinhibition have been modest. One potential explanation is that tumorsuse nonoverlapping immunosuppressive mechanisms to facilitate immuneescape. Accordingly, improved compositions and methods for reducingtumor-mediated immunosuppression are urgently required.

SUMMARY OF THE INVENTION

The present invention provides isolated binding molecules orantigen-binding fragments thereof which specifically bind to CD73. Insome aspects, such CD73-binding molecules are, e.g., antibodies orantigen-binding fragments thereof. In particular embodiments, anti-CD73antibodies of the invention (e.g., MEDI9447) is useful for reducingtumor-mediated immunosuppression.

In one aspect, the invention generally provides a method of inhibitingtumor growth in a subject, the method comprising administering to asubject in need thereof an anti-CD73 antibody, or an antigen-bindingfragment thereof, and an A2A receptor inhibitor.

In another aspect, the invention provides a method of increasing ananti-tumor immune response in a subject, the method comprisingadministering to a subject in need thereof an anti-CD73 antibody, or anantigen-binding fragment thereof, and an A2A receptor inhibitor to thesubject.

In a further aspect, the invention provides a method of treating a tumorin a subject, the method comprising administering to a subject in needthereof an anti-CD73 antibody, or an antigen-binding fragment thereof,and an A2A receptor inhibitor.

In one or more embodiments of any of the aspects of the inventionprovided the anti-CD73 antibody is MEDI9447 or an antigen-bindingfragment thereof. In another embodiment the anti-CD73 antibody isPhen0203 hIgG1 or an antigen-binding fragment thereof. In yet anotherembodiment the A2A receptor inhibitor is SCH58261. In additionalembodiments the CD73 inhibitor is adenosine5′-(α,β-methylene)diphosphate (APCP). In yet another embodiment theanti-CD73 antibody is MEDI9447 or an antigen-binding fragment thereofand the A2A receptor inhibitor is SCH58261. In additional embodimentsthe anti-CD73 antibody is Phen0203 hIgG1 or an antigen-binding fragmentthereof and the A2A receptor inhibitor is SCH58261. In yet anotherembodiment the anti-CD73 antibody or antigen-binding fragment thereof orthe adenosine receptor inhibitor (A2ARi) are administered concurrently.In further embodiments anti-CD73 antibody is administered prior to theadenosine receptor inhibitor (A2ARi). In other embodiments the adenosinereceptor inhibitor (A2ARi) is administered prior to the anti-CD73antibody. In other embodiments the tumor is a breast cancer, hormonallymediated breast cancer, triple negative breast cancer, colon carcinoma,colorectal cancer, lung cancer, melanoma, non-small cell carcinoma,lymphoma, Hodgkin's and non-Hodgkin's lymphoma, Burkitt's lymphoma, andsarcoma. In another embodiment the method results in an increase inoverall survival as compared to the administration of any one of theanti-CD73 antibody or the A2A receptor inhibitor alone. In otherembodiments the method induces or increases a tumor-specific immuneresponse. In another embodiment the method reduces the immunosuppressiveeffects of a AMP/CD73/adenosine pathway. In further embodiments themethod reduces metastasis or reduces the propensity of the tumor tometastasize relative to the administration of either the anti-CD73antibody or the adenosine receptor inhibitor (A2ARi) alone. In yetanother embodiment the method reduces the number of metastases withinthe subject. In certain embodiments the subject is a human patient. Inyet another embodiment the tumor is a CD73 overexpressing tumor. Inother embodiments the cancer has a prometastatic phenotype.

In another aspect, the invention provides a kit for increasinganti-tumor activity, the kit comprising an anti-CD73 antibody orantigen-binding fragment thereof and an A2A receptor inhibitor. In anembodiment of this aspect, the anti-CD73 antibody is MEDI9447 or anantigen-binding fragment thereof. In another embodiment of this aspect,the anti-CD73 antibody is Phen0203 hIgG1 or an antigen-binding fragmentthereof. In yet another embodiment of this aspect, the A2A receptorinhibitor is SCH58261. In another embodiment the anti-CD73 antibody isMEDI9447 or an antigen-binding fragment thereof and the A2A receptorinhibitor is SCH58261. In additional embodiments the anti-CD73 antibodyis Phen0203 hIgG1 or an antigen-binding fragment thereof and the A2Areceptor inhibitor is SCH58261.

In another aspect, the invention provides a pharmaceutical formulationcomprising an effective amount an anti-CD73 antibody or antigen-bindingfragment thereof and an A2A receptor inhibitor. In an embodiment of thisaspect the anti-CD73 antibody is MEDI9447 or an antigen-binding fragmentthereof. In another embodiment the anti-CD73 antibody is Phen0203 hIgG1or an antigen-binding fragment thereof. In yet another embodiment theA2A receptor inhibitor is SCH58261. In additional embodiments theanti-CD73 antibody is MEDI9447 or an antigen-binding fragment thereofand the A2A receptor inhibitor is SCH58261. In certain embodiments theanti-CD73 antibody is Phen0203 hIgG1 or an antigen-binding fragmentthereof and the A2A receptor inhibitor is SCH58261.

BRIEF DESCRIPTION OF THE DRAWINGS/FIGURES

FIG. 1A shows the nucleotide sequence (SEQ ID NO: 22) and amino acidtranslation (SEQ ID NO: 21) of MEDI9447 VH domain with CDRs shown basedon Kabat numbering convention.

FIG. 1B shows the nucleotide sequence (SEQ ID NO: 24) and amino acidtranslation (SEQ ID NO: 23) of MEDI9447 VL domain with CDRs shown basedon Kabat numbering convention.

FIG. 1C an alignment of MEDI9447 VH (SEQ ID NO: 21) with closest humanVH and JH germline sequences (SEQ ID NO: 147). CDRs based on Kabatnumbering convention are highlighted and residues different fromgermline sequences are boxed.

FIG. 1D shows an alignment of MEDI9447 VL (SEQ ID NO: 23) with closesthuman VL and JL germline sequences (SEQ ID NO: 148). CDRs based on Kabatnumbering convention are highlighted and residues different fromgermline sequences are boxed.

FIG. 2 provides two graph showing antibody-mediated internalization of acytotoxic FabZAP reagent into MDA-MB-231 cells and 4T1 cells, where theantibodies are MEDI9447 and the control antibody R347.

FIG. 3A is a graph showing inhibition of 5′ ectonucleotidase by theanti-CD73 antibody MEDI9447.

FIG. 3B is a graph showing inhibition of AMP hydrolysis by anti-CD73antibody CD370010.

FIG. 4 is a graph showing that MEDI9447 inhibited tumor growth in a CT26syngeneic tumor model. Murine CT26 tumor cells were implantedsubcutaneously on the right flank of female Balb/C mice. Tumors wereallowed to grow for 3 days and treated with MEDI9447 or an isotypecontrol twice weekly for two weeks. At Day 16, tumors were harvested forflow cytometry analysis.

FIG. 5 is a graph showing that MEDI9447 inhibited tumor-infiltratingmyeloid-derived suppressor cells (MDSCs). MEDI9447-treated CT26tumor-bearing mice were sacrificed and tumors were harvested at studyDay 16. Tumors were disassociated into single cells, stained for CD45and MDSC markers, and analyzed by flow cytometry.

FIG. 6 includes six spider plots showing the effect of MEDI9447 mIgG1,anti-PD-1 or the combination on tumor volume. Control antibodies includerIgG2a, which is a Rat IgG2a control monoclonal rat antibody specificfor E. coli β-galactosidase (β-Gal), and Isotype control murine IgG1.Tumor volumes from each group of animals were plotted for individualanimals out to study day 40. No control group mice were tumor free bythe end of the 40 day study period. Anti-CD73 treatment alone resultedin 10% tumor free animals at the end of study. Anti-PD-1 treatment alonealso resulted in 10% tumor free animals at the end of study. Remarkably,the combination of anti-CD73 and anti-PD treatment resulted in 60% tumorfree mice. None of the control group mice were tumor free by the end ofthe study.

FIG. 7 is a graph showing the effect of MEDI9447 mIgG1, anti-PD-1 or thecombination on tumor volume.

FIG. 8 is a graph showing the effect of MEDI9447 mIgG1, anti-PD-1 or thecombination on survival.

FIG. 9 is a graph showing the effect of Phen0203 hIgG1 antibody onAMP-mediated suppression of CD4+CD25-T-cell proliferation.

FIG. 10 is a graph showing the effect of SCH58261 on AMP-mediatedsuppression of CD4⁺CD25⁻ T cell proliferation.

FIG. 11 is a graph showing the effect of anti-CD73 and SH58261, eitheralone or in combination, on IFNγ supernatant levels in a mixed leukocytereaction.

FIG. 12 is a graph showing the effect of anti-CD73 and SH58261, eitheralone or in combination, on TNFα supernatant levels in a mixed leukocytereaction.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides isolated binding molecules orantigen-binding fragments thereof which specifically bind to CD73. Insome aspects, such molecules are antibodies and antigen-bindingfragments thereof that specifically bind to CD73. Relatedpolynucleotides, vectors, pharmaceutical compositions comprising theanti-CD73 antibodies or antigen-binding fragments thereof, are alsoprovided. Also provided are methods of making as well as methods ofusing the anti-CD73 antibodies and antigen-binding fragments disclosedherein, for example, diagnostic methods and methods of treating cancerin a subject (as direct therapy, adjuvant therapy, or in combinationtherapy). The invention also provides antibody-drug conjugates derivedfrom the CD73 binding molecules disclosed herein.

In order that the present disclosure can be more readily understood,certain terms are first defined. Additional definitions are set forththroughout the detailed description.

I. DEFINITIONS

Before describing the present invention in detail, it is to beunderstood that this invention is not limited to specific compositionsor process steps, as such can vary. As used in this specification andthe appended claims, the singular forms “a”, “an” and “the” includeplural referents unless the context clearly dictates otherwise. Theterms “a” (or “an”), as well as the terms “one or more,” and “at leastone” can be used interchangeably herein.

Furthermore, “and/or” where used herein is to be taken as specificdisclosure of each of the two specified features or components with orwithout the other. Thus, the term and/or” as used in a phrase such as “Aand/or B” herein is intended to include “A and B,” “A or B,” “A”(alone), and “B” (alone). Likewise, the term “and/or” as used in aphrase such as “A, B, and/or C” is intended to encompass each of thefollowing aspects: A, B, and C; A, B, or C; A or C; A or B; B or C; Aand C; A and B; B and C; A (alone); B (alone); and C (alone).

Unless defined otherwise, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this disclosure is related. For example, the ConciseDictionary of Biomedicine and Molecular Biology, Juo, Pei-Show, 2nd ed.,2002, CRC Press; The Dictionary of Cell and Molecular Biology, 3rd ed.,1999, Academic Press; and the Oxford Dictionary Of Biochemistry AndMolecular Biology, Revised, 2000, Oxford University Press, provide oneof skill with a general dictionary of many of the terms used in thisdisclosure.

Units, prefixes, and symbols are denoted in their Systeme Internationalde Unites (SI) accepted form. Numeric ranges are inclusive of thenumbers defining the range. Unless otherwise indicated, amino acidsequences are written left to right in amino to carboxy orientation. Theheadings provided herein are not limitations of the various aspects,which can be had by reference to the specification as a whole.Accordingly, the terms defined immediately below are more fully definedby reference to the specification in its entirety.

It is understood that wherever aspects are described herein with thelanguage “comprising,” otherwise analogous aspects described in terms of“consisting of” and/or “consisting essentially of” are also provided.

Amino acids are referred to herein by either their commonly known threeletter symbols or by the one-letter symbols recommended by the IUPAC-IUBBiochemical Nomenclature Commission. Nucleotides, likewise, are referredto by their commonly accepted single-letter codes.

The term “CD73 polypeptide” as used herein refers to the CD73 (Clusterof Differentiation 73) protein, also referred to as 5′-nucleotidase(5′-NT) or ecto-5′-nucleotidase in the literature, which is encoded bythe NT5E gene. See, e.g., Misumi et al. Eur. J. Biochem. 191(3): 563-9(1990). The respective sequences of the human and murine forms of CD73are available at the Uniprot database under accession numbers P21589 andQ61503, respectively.

An exemplary CD73 polypeptide is provided below:

>sp|P21589|5NTD_HUMAN 5′-nucleotidase OS = Homo sapiens GN = NT5E PE =1 SV = 1 (SEQ ID NO: 130)MCPRAARAPATLLLALGAVLWPAAGAWELTILHTNDVHSRLEQTSEDSSKCVNASRCMGGVARLFTKVQQIRRAEPNVLLLDAGDQYQGTIWFTVYKGAEVAHFMNALRYDAMALGNHEFDNGVEGLIEPLLKEAKFPILSANIKAKGPLASQISGLYLPYKVLPVGDEVVGIVGYTSKETPFLSNPGTNLVFEDEITALQPEVDKLKTLNVNKIIALGHSGFEMDKLIAQKVRGVDVVVGGHSNTFLYTGNPPSKEVPAGKYPFIVTSDDGRKVPVVQAYAFGKYLGYLKIEFDERGNVISSHGNPILLNSSIPEDPSIKADINKWRIKLDNYSTQELGKTIVYLDGSSQSCRFRECNMGNLICDAMINNNLRHTDEMFWNHVSMCILNGGGIRSPIDERNNGTITWENLAAVLPFGGTFDLVQLKGSTLKKAFEHSVHRYGQSTGEFLQVGGIHVVYDLSRKPGDRVVKLDVLCTKCRVPSYDPLKMDEVYKVILPNFLANGGDGFQMIKDELLRHDSGDQDINVVSTYISKMKVIYPAVEGRIKFSTGSHCHGSFSLIFLSLWAVIFVLYQ

Soluble and membrane-bound forms of CD73 have been identified. SeeKlemens et al, Biochem. Biophys. Res. Commun. 172(3):1371-7 (1990). Inaddition, several different isoenzymes have been identified. See Rosi etal. Life Sci. 62(25):2257-66 (1998). The full-length CD73 proteincomprises 574 amino acids. The mature CD73 protein is produced afterremoval of a signal sequence (positions 1 to 26) and the C-terminalregion of the propeptide (positions 550-574). In addition, amino acids404 to 453 are removed in isoform 2 of CD73 after alternative splicing.Natural variants are also known, for example, variant C358Y, variantT376A, and variant M379T. See Misumi et al., Eur. J. Biochem.191:563-569 (1990); Otsuki et al. DNA Res. 12:117-126 (2005); Mungall etal. Nature 425:805-811 (2003); Hansen et al. Gene 167:307-312 (1995);Klemens et al. Biochem. Biophys. Res. Commun. 172:1371-1377 (1990);Knapp et al. Structure 20:2161-2173 (2012); or St. Hilaire et al. N.Engl. J. Med. 364:432-442 (2011), all of which are herein incorporatedby reference in their entireties.

Accordingly, the CD73-binding molecules disclosed herein can be used forexample to treat or diagnose cancer (e.g., breast cancer (includinghormonally mediated breast cancer, see, e.g., Innes et al. (2006) Br. J.Cancer 94:1057-1065), triple negative breast cancer, colon carcinoma,colorectal cancer, lung cancer, melanoma, non-small cell carcinoma,lymphoma, Hodgkin's and non-Hodgkin's lymphoma, Burkitt's lymphoma, andsarcoma). In addition, the measurement of the levels of CD73 in a samplefrom a patient (e.g., a tissue fluid) using the CD73-binding moleculesdisclosed herein can be used for monitoring the development of the abovedescribed diseases, for assessing the efficacy of therapies, to electpatients for treatment with a particular therapy, or to take medicaldecisions, for example, commencing, ending, interrupting, or modifying acertain treatment.

The term “adenosine A2A receptor (ADORA2A) polypeptide” as used hereinrefers to a protein having at least about 85% amino acid sequenceidentity to NP_000666 or a fragment thereof and having adenosine bindingand G-protein signaling activity. The respective sequences of the humanand murine forms of adenosine A2A receptor are available at the Uniprotdatabase under accession numbers P29274 and Q60613, respectively.

An exemplary adenosine A2A receptor polypeptide is provided below:

>sp|P29274|AA2AR_HUMAN Adenosine receptor A2a OS = Homo sapiens GN =ADORA2A PE = 1 SV = 2 (SEQ ID NO: 131)MPIMGSSVYITVELAIAVLAILGNVLVCWAVWLNSNLQNVTNYFVVSLAAADIAVGVLAIPFAITITGFCAACHGCLFIACFVLVLTQSSIFSLLAIAIDRYIAIRIPLRYNGLVTGTRAKGIIAICWVLSFAIGLTPMLGWNNCGQPKEGKNHSQGCGEGQVACLFEDVVPMNYMVYFNFFACVLVPLLLMLGVYLRIFLAARRQLKQMESQPLPGERARSTLQKEVHAAKSLAIIVGLFALCWLPLHIINCFTFFCPDCSHAPLWLMYLAIVLSHTNSVVNPFIYAYRIREFRQTFRKIIRSHVLRQQEPFKAAGTSARVLAAHGSDGEQVSLRLNGHPPGVWANGSAPHPERRPNGYALGLVSGGSAQESQGNTGLPDVELLSHELKGVCPEPPGLD DPLAQDGAGVS

By “SCH58261” is meant a small compound having the following structuralformula:

CAS 160098-96-4, and having adenosine A2A receptor binding andinhibitory activity.

By “adenosine A2A receptor inhibitor (A2ARi)” is meant an agent thatinhibits the G protein signaling activity of an adenosine A2A receptor.In one embodiment, inhibition of A2A receptor activity is measured bymeasuring TNFα secretion in a mixed lymphocyte stimulation assay, wherean increase in TNFα indicates inhibition of adenosine A2A receptoractivity.

By “adenosine 5′-(α,β-methylene)diphosphate (APCP)” is meant a smallcompound having the following structural formula:

CAS 3768-14-7, and having CD73 enzyme inhibitory activity.

The terms “inhibit,” “block,” “suppress,” and grammatical variantsthereof are used interchangeably herein and refer to any statisticallysignificant decrease in biological activity, including full blocking ofthe activity. For example, “inhibition” can refer to a decrease of about10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90% or 100% in biologicalactivity. Accordingly, when the terms “inhibition” or “suppression” areapplied to describe, e.g., an effect on the enzymatic activity of CD73,the term refers to the ability of an anti-CD73 antibody orantigen-binding fragment thereof to statistically significantly decreasethe 5′-nucleotidase activity of CD73 (catabolizing the hydrolysis ofadenosine monophosphate, AMP, to adenosine), relative to theCD73-mediated 5′-nucleotidase activity in an untreated (control) cell.The cell which expresses CD73 can be a naturally occurring cell or cellline (e.g., a cancer cell) or can be recombinantly produced byintroducing a nucleic acid encoding CD73 into a host cell. In someaspects, an anti-CD73 antibody or antigen-binding fragment thereof canstatistically significantly decrease the 5′-nucleotidase activity of asoluble form of CD73 in a biological fluid. In one aspect, the anti-CD73binding molecule, e.g., an antibody or antigen-binding fragment thereofinhibits CD73-mediated 5′-nucleotidase activity by at least 10%, atleast 15%, or at least 20%, at least 25%, or at least 30%, at least 35%,or at least 40%, at least 45%, or at least 50%, at least 55%, or atleast 60%, at least 65%, or at least 70%, at least 75%, or at least 80%,at least 85%, or at least 90%, at least 95%, or about 100%, asdetermined, for example, by the methods described in the Examples infra,and/or methods known in the art.

The term “suppress CD73 activity,” as used herein, refer to the abilityof anti-CD73 binding molecule, e.g., an antibody or antigen-bindingfragment thereof to statistically significantly decrease CD73-dependent5′-nucleotidase activity in a cell expressing CD73 or a samplecontaining CD73. In some aspects, the suppression of CD73 activity canbe a decrease of at least 10%, or at least 15%, or at least 20%, or atleast 25%, or at least 30%, or at least 35%, or at least 40%, or atleast 45%, or at least 50%, or at least 55%, or at least 60%, or atleast 65%, or at least 70%, or at least 75%, or at least 80%, or atleast 85%, or at least 90%, or at least 95%, or about 100% when cells ora sample are contacted with an anti-CD73 binding molecule, e.g., anantibody or antigen-binding fragment thereof of the present disclosure,relative to the CD73 activity measured in the absence of the anti-CD73binding molecule, e.g., an antibody or antigen-binding fragment thereof(control conditions).

The terms “antibody” or “immunoglobulin,” as used interchangeablyherein, include whole antibodies and any antigen-binding fragment orsingle chains thereof.

A typical antibody comprises at least two heavy (H) chains and two light(L) chains interconnected by disulfide bonds. Each heavy chain iscomprised of a heavy chain variable region (abbreviated herein as VH orV_(H)) and a heavy chain constant region. The heavy chain constantregion is comprised of three domains, CH1, CH2, and CH3. Each lightchain is comprised of a light chain variable region (abbreviated hereinas VL or V_(L)) and a light chain constant region. The light chainconstant region is comprised of one domain, CL. The VH and VL regionscan be further subdivided into regions of hypervariability, termedComplementarity Determining Regions (CDR), interspersed with regionsthat are more conserved, termed framework regions (FW). Each VH and VLis composed of three CDRs and four FWs, arranged from amino-terminus tocarboxy-terminus in the following order: FW1, CDR1, FW2, CDR2, FW3,CDR3, FW4. The variable regions of the heavy and light chains contain abinding domain that interacts with an antigen. The constant regions ofthe antibodies can mediate the binding of the immunoglobulin to hosttissues or factors, including various cells of the immune system (e.g.,effector cells) and the first component (Clq) of the classicalcomplement system. Exemplary antibodies of the present disclosureinclude anti-CD73 antibodies (original and germlined), affinityoptimized clones, optimized antibodies lacking ADCC, conjugatedantibodies (e.g., ADC), and other optimized antibodies (e.g., serumhalf-life-optimized antibodies including, for example, YTE mutations,see Dall'Acqua et al., J. Biol. Chem. 281:23514-24 (2006) and U.S. Pat.No. 7,083,784, which are hereby incorporated by reference in theirentireties).

The term “germlining” means that amino acids at specific positions in anantibody are mutated back to those in the germ line.

The term “antibody” means an immunoglobulin molecule that recognizes andspecifically binds to a target, such as a protein, polypeptide, peptide,carbohydrate, polynucleotide, lipid, or combinations of the foregoingthrough at least one antigen recognition site within the variable regionof the immunoglobulin molecule. As used herein, the term “antibody”encompasses intact polyclonal antibodies, intact monoclonal antibodies,antibody fragments (such as Fab, Fab′, F(ab′)2, and Fv fragments),single chain Fv (scFv) mutants, multispecific antibodies such asbispecific antibodies generated from at least two intact antibodies,chimeric antibodies, humanized antibodies, human antibodies, fusionproteins comprising an antigen determination portion of an antibody, andany other modified immunoglobulin molecule comprising an antigenrecognition site so long as the antibodies exhibit the desiredbiological activity.

An antibody can be of any the five major classes of immunoglobulins:IgA, IgD, IgE, IgG, and IgM, or subclasses (isotypes) thereof (e.g.IgG1, IgG2, IgG3, IgG4, IgA1 and IgA2), based on the identity of theirheavy-chain constant domains referred to as alpha, delta, epsilon,gamma, and mu, respectively. The different classes of immunoglobulinshave different and well known subunit structures and three-dimensionalconfigurations. Antibodies can be naked or conjugated to other moleculessuch as toxins, radioisotopes, etc. to form ADCs.

A “blocking” antibody or an “antagonist” antibody is one which inhibitsor reduces biological activity of the antigen it binds, such as CD73. Ina certain aspect blocking antibodies or antagonist antibodiessubstantially or completely inhibit the biological activity of theantigen. Desirably, the biological activity is reduced by at least 10%,at least 15%, at least 20%, at least 25%, at least 30%, at least 35%, atleast 40%, at least 45%, at least 50%, at least 55%, at least 60%, atleast 65%, at least 70%, at least 75%, at least 80%, at least 85%, atleast 90%, at least 95%, or even 100%.

The terms “CD73 antibody,” “antibody that binds to CD73” or “anti-CD73”refers to an antibody or antigen-binding fragment thereof that iscapable of selectively binding CD73. In one embodiment an anti-CD73antibody binds CD73 with sufficient affinity such that the molecule isuseful as a therapeutic agent or diagnostic reagent in targeting CD73.The extent of binding of an anti-CD73 antibody to an unrelated, non-CD73protein is less than about 10% of the binding of the antibody to CD73 asmeasured, e.g., by a radioimmunoassay (RIA), BIACORE™ (using recombinantCD73 as the analyte and antibody as the ligand, or vice versa), or otherbinding assays known in the art. In certain aspects, an antibody thatbinds to CD73 has a dissociation constant (K_(D)) of ≦1 μM, ≦100 nM, ≦10nM, ≦1 nM, ≦0.1 nM, ≦10 pM, ≦1 pM, or ≦0.1 pM. The term “anti-CD73” alsobroadly encompasses molecules comprising, e.g., the CDRs of theantibodies disclosed herein incorporated into a scaffold. Thus, thephrase “isolated binding molecule or antigen-binding fragment thereofwhich specifically binds to CD73” would refer not only to antibodies andantigen-binding fragments thereof, but also would refer to a moleculecomprising, for example, one or more scaffolds (such as a fibronectinIII domain from fibronectin or tenascin-3) incorporating the CDRs of theantibodies disclosed herein.

In one embodiment, an anti-CD73 antibody refers to an antibody inIgG1-TM format such that the IgG1 Fc domain comprises mutations L234,L235E and P331, binds soluble and cell-surface displayed CD73, andinhibits CD73 enzymatic activity. FIGS. 1A-D provide the nucleotide andamino acid sequences of MEDI9447 VH and VL domains.

The term “antigen-binding fragment” refers to a molecule comprising aportion of an intact antibody, and in particular refers to a moleculecomprising the antigenic determining variable regions of an intactantibody. It is known in the art that the antigen-binding function of anantibody can be performed by fragments of a full-length antibody.Examples of antibody fragments include, but are not limited to Fab,Fab′, F(ab′)2, and Fv fragments, linear antibodies, single chainantibodies, and multispecific antibodies formed from antibody fragments.

A “monoclonal antibody” refers to a homogeneous antibody populationinvolved in the highly specific recognition and binding of a singleantigenic determinant, or epitope. This is in contrast to polyclonalantibodies that typically include different antibodies directed againstdifferent antigenic determinants.

The term “monoclonal antibody” encompasses both intact and full-lengthmonoclonal antibodies as well as antibody fragments (such as Fab, Fab′,F(ab′)2, Fv), single chain variable fragments (scFv), fusion proteinscomprising an antibody portion, and any other modified immunoglobulinmolecule comprising an antigen recognition site. Furthermore,“monoclonal antibody” refers to such antibodies made in any number ofways including, but not limited to, by hybridoma, phage selection,recombinant expression, and transgenic animals (e.g., expression of ahuman antibody in a transgenic mouse).

The term “humanized antibody” refers to an antibody derived from anon-human (e.g., murine) immunoglobulin, which has been engineered tocontain minimal non-human (e.g., murine) sequences. Typically, humanizedantibodies are human immunoglobulins in which residues from the CDRs arereplaced by residues from the CDR of a non-human species (e.g., mouse,rat, rabbit, or hamster) that have the desired specificity, affinity,and capability (Jones et al., 1986, Nature, 321:522-525; Riechmann etal., 1988, Nature, 332:323-327; Verhoeyen et al., 1988, Science,239:1534-1536). In some instances, the framework (FW) amino acidresidues of a human immunoglobulin are replaced with the correspondingresidues in an antibody from a non-human species that has the desiredspecificity, and/or affinity, and/or capability.

The humanized antibody can be further modified by the substitution ofadditional residues either in the Fv framework region and/or within thereplaced non-human residues to refine and optimize antibody specificity,affinity, and/or capability. In general, the humanized antibody willcomprise substantially all of at least one, and typically two or three,variable domains containing all or substantially all of the CDR regionsthat correspond to the non-human immunoglobulin, whereas all orsubstantially all of the FR regions are those of a human immunoglobulinconsensus sequence. The humanized antibody can also comprise at least aportion of an immunoglobulin constant region or domain (Fc), typicallythat of a human immunoglobulin. Examples of methods used to generatehumanized antibodies are described in U.S. Pat. No. 5,225,539 or5,639,641.

A “variable region” of an antibody refers to the variable region of theantibody light chain or the variable region of the antibody heavy chain,either alone or in combination. The variable regions of the heavy andlight chain each consist of four FW regions connected by three CDRregions. The CDRs in each chain are held together in close proximity bythe FW regions and, with the CDRs from the other chain, contribute tothe formation of the antigen-binding site of antibodies. There are atleast two techniques for determining CDRs: (1) an approach based oncross-species sequence variability (i.e., Kabat et al. Sequences ofProteins of Immunological Interest, (5th ed., 1991, National Institutesof Health, Bethesda Md.)); and (2) an approach based on crystallographicstudies of antigen-antibody complexes (Al-lazikani et al. (1997) J.Molec. Biol. 273:927-948)). In addition, combinations of these twoapproaches are sometimes used in the art to determine CDRs.

The Kabat numbering system is generally used when referring to a residuein the variable domain (approximately residues 1-107 of the light chainand residues 1-113 of the heavy chain) (e.g., Kabat et al., Sequences ofImmunological Interest, 5th Ed. Public Health Service, NationalInstitutes of Health, Bethesda, Md. (1991)).

The phrases “amino acid position numbering as in Kabat,” “Kabatposition,” and grammatical variants thereof refer to the numberingsystem used for heavy chain variable domains or light chain variabledomains of the compilation of antibodies in Kabat et al., Sequences ofProteins of Immunological Interest, 5th Ed. Public Health Service,National Institutes of Health, Bethesda, Md. (1991). Using thisnumbering system, the actual linear amino acid sequence can containfewer or additional amino acids corresponding to a shortening of, orinsertion into, a FW or CDR of the variable domain. For example, a heavychain variable domain can include a single amino acid insert (residue52a according to Kabat) after residue 52 of H2 and inserted residues(e.g., residues 82a, 82b, and 82c, etc. according to Kabat) after heavychain FW residue 82.

TABLE 1 Loop Kabat AbM Chothia L1 L24-L34 L24-L34 L24-L34 L2 L50-L56L50-L56 L50-L56 L3 L89-L97 L89-L97 L89-L97 H1 H31-H35B H26-H35B H26-H32. . . 34 (Kabat Numbering) H1 H31-H35 H26-H35 H26-H32 (ChothiaNumbering) H2 H50-H65 H50-H58 H52-H56 H3 H95-H102 H95-H102 H95-H102

The Kabat numbering of residues can be determined for a given antibodyby alignment at regions of homology of the sequence of the antibody witha “standard” Kabat numbered sequence. Chothia refers instead to thelocation of the structural loops (Chothia and Lesk, J. Mol. Biol.196:901-917 (1987)). The end of the Chothia CDR-H1 loop when numberedusing the Kabat numbering convention varies between H32 and H34depending on the length of the loop (this is because the Kabat numberingscheme places the insertions at H35A and H35B; if neither 35A nor 35B ispresent, the loop ends at 32; if only 35A is present, the loop ends at33; if both 35A and 35B are present, the loop ends at 34). The AbMhypervariable regions represent a compromise between the Kabat CDRs andChothia structural loops, and are used by Oxford Molecular's AbMantibody modeling software.

IMGT (ImMunoGeneTics) also provides a numbering system for theimmunoglobulin variable regions, including the CDRs. See e.g., Lefranc,M. P. et al., Dev. Comp. Immunol. 27: 55-77(2003), which is hereinincorporated by reference. The IMGT numbering system was based on analignment of more than 5,000 sequences, structural data, andcharacterization of hypervariable loops and allows for easy comparisonof the variable and CDR regions for all species. According to the IMGTnumbering schema VH-CDR1 is at positions 26 to 35, VH-CDR2 is atpositions 51 to 57, VH-CDR3 is at positions 93 to 102, VL-CDR1 is atpositions 27 to 32, VL-CDR2 is at positions 50 to 52, and VL-CDR3 is atpositions 89 to 97.

The EU index or EU numbering system is based on the sequential numberingof the first human IgG sequenced (the EU antibody). Because the mostcommon reference for this convention is the Kabat sequence manual (Kabatet al., 1991), the EU index is sometimes erroneously used synonymouslywith the Kabat index. The EU index does not provide insertions anddeletions, and thus in some cases comparisons of IgG positions acrossIgG subclass and species can be unclear, particularly in the hingeregions. Nonetheless, the convention has sufficed at enablingstraightforward comparison between Fc regions in numerous Fc structurefunction studies. Accordingly, the numbering scheme used forsubstitutions and insertions in Fc regions in this specification is theEU index as in Kabat. In contrast, the numbering scheme used for thevariable regions (VH and VL) in this specification is the regular Kabatnumbering.

As used throughout the specification the VH CDRs sequences describedcorrespond to the classical Kabat numbering locations, namely KabatVH-CDR1 is at positions 31-35, VH-CDR2 is a positions 50-65, and VH-CDR3is at positions 95-102. VL-CDR1, VL-CDR2 and VL-CDR3 also correspond toclassical Kabat numbering locations, namely positions 24-34, 50-56 and89-97, respectively.

As used herein the Fc region includes the polypeptides comprising theconstant region of an antibody excluding the first constant regionimmunoglobulin domain. Thus, Fc refers to the last two constant regionimmunoglobulin domains of IgA, IgD, and IgG, and the last three constantregion immunoglobulin domains of IgE and IgM, and the flexible hingeN-terminal to these domains. For IgA and IgM Fc can include the J chain.For IgG, Fc comprises immunoglobulin domains Cgamma2 and Cgamma3 (Cγ2and Cγ3) and the hinge between Cgamma1 (Cγ1) and Cgamma2 (Cγ2).

Although the boundaries of the Fc region can vary, the human IgG heavychain Fc region is usually defined to comprise residues C226 or P230 toits carboxyl-terminus, wherein the numbering is according to the EUindex as set forth in Kabat (Kabat et al., Sequences of Proteins ofImmunological Interest, 5th Ed. Public Health Service, NationalInstitutes of Health, Bethesda, Md. (1991)). Fc can refer to this regionin isolation, or this region in the context of an antibody, antibodyfragment, or Fc fusion protein. Polymorphisms have been observed at anumber of different Fc positions, including but not limited to positions270, 272, 312, 315, 356, and 358 as numbered by the EU index, and thusslight differences between the presented sequence and sequences in theprior art can exist.

The term “human antibody” means an antibody produced by a human or anantibody having an amino acid sequence corresponding to an antibodyproduced by a human made using any technique known in the art (e.g.,recombinant expression in cultures cells, or expression in transgenicanimals). Thus, the term human antibody also encompasses an antibodyhaving an amino acid sequence corresponding to an antibody originallyproduced by a human (or an engineered variant or derivative thereof) butexpressed in a non-human system (e.g., produced by chemical synthesis;recombinantly expressed in microbial, mammal, or insect cells; orexpressed in an animal subject). Accordingly, an antibody obtained froma human subject or from human cells (e.g., hybridoma or cell lineexpressing a recombinant antibody or fragment thereof) and subsequentlyexpressed in an animal, e.g., mice, is considered a human antibody. Thisdefinition of a human antibody includes intact or full-lengthantibodies, fragments thereof, and/or antibodies comprising at least onehuman heavy and/or light chain polypeptide such as, for example, anantibody comprising murine light chain and human heavy chainpolypeptides.

The term “chimeric antibodies” refers to antibodies wherein the aminoacid sequence of the immunoglobulin molecule is derived from two or moreanimal species. Typically, the variable region of both light and heavychains corresponds to the variable region of antibodies derived from onespecies of mammals (e.g., mouse, rat, rabbit, etc.) with the desiredspecificity, and/or affinity, and/or capability while the constantregions are homologous to the sequences in antibodies derived fromanother specie (usually human) to avoid eliciting an immune response inthat species.

The term “epitope” as used herein refers to an antigenic proteindeterminant capable of binding to a CD73 antibody or CD73 bindingmolecule disclosed herein. Epitopes usually consist of chemically activesurface groupings of molecules such as amino acids or sugar side chainsand usually have specific three dimensional structural characteristics,as well as specific charge characteristics. The part of an antibody orbinding molecule that recognizes the epitope is called a paratope. Theepitopes of protein antigens are divided into two categories,conformational epitopes and linear epitopes, based on their structureand interaction with the paratope. A conformational epitope is composedof discontinuous sections of the antigen's amino acid sequence. Theseepitopes interact with the paratope based on the 3-D surface featuresand shape or tertiary structure of the antigen. By contrast, linearepitopes interact with the paratope based on their primary structure. Alinear epitope is formed by a continuous sequence of amino acids fromthe antigen.

The term “antibody binding site” refers to a region in the antigen(e.g., CD73) comprising a continuous or discontinuous site (i.e., anepitope) to which a complementary antibody specifically binds. Thus, theantibody binding site can contain additional areas in the antigen whichare beyond the epitope and which can determine properties such asbinding affinity and/or stability, or affect properties such as antigenenzymatic activity or dimerization. Accordingly, even if two antibodiesbind to the same epitope within an antigen, if the antibody moleculesestablish distinct intermolecular contacts with amino acids outside ofthe epitope, such antibodies are considered to bind to distinct antibodybinding sites.

“Binding affinity” generally refers to the strength of the sum total ofnon-covalent interactions between a single binding site of a molecule(e.g., an antibody) and its binding partner (e.g., an antigen). Unlessindicated otherwise, as used herein, “binding affinity” refers tointrinsic binding affinity which reflects a 1:1 interaction betweenmembers of a binding pair (e.g., antibody and antigen). The affinity ofa molecule X for its partner Y can generally be represented by thedissociation constant (K_(D)). Affinity can be measured by commonmethods known in the art, including those described herein. Low-affinityantibodies generally bind antigen slowly and tend to dissociate readily,whereas high-affinity antibodies generally bind antigen faster and tendto remain bound longer. A variety of methods of measuring bindingaffinity are known in the art, any of which can be used for purposes ofthe present disclosure.

“Potency” is normally expressed as an IC₅₀ value, in nM unless otherwisestated. IC₅₀ is the median inhibitory concentration of anantigen-binding molecule. In functional assays, IC₅₀ is theconcentration that reduces a biological response by 50% of its maximum.In ligand-binding studies, IC₅₀ is the concentration that reducesreceptor binding by 50% of maximal specific binding level. IC₅₀ can becalculated by any number of means known in the art. Improvement inpotency can be determined by measuring, e.g., against a parent antibody(for example, the parent antibody prior to germlining or the parentantibody prior to affinity optimization).

The fold improvement in potency for the antibodies or polypeptides ofthe present disclosure as compared to a parent antibody can be at leastabout 2-fold, at least about 4-fold, at least about 6-fold, at leastabout 8-fold, at least about 10-fold, at least about 15-fold, at leastabout 20-fold, at least about 25-fold, at least about 30-fold, at leastabout 40-fold, at least about 50-fold, at least about 60-fold, at leastabout 70-fold, at least about 80-fold, at least about 90-fold, at leastabout 100-fold, at least about 110-fold, at least about 120-fold, atleast about 130-fold, at least about 140-fold, at least about 150-fold,at least about 160-fold, at least about 170-fold, or at least about180-fold or more.

“Antibody-dependent cell-mediated cytotoxicity” or “ADCC” refers to aform of cytotoxicity in which secreted immunoglobulins bound onto Fcreceptors (FcRs) present on certain cytotoxic cells (e.g., NaturalKiller (NK) cells, neutrophils, and macrophages) enable these cytotoxiceffector cells to bind specifically to an antigen-bearing target celland subsequently kill the target cell with cytotoxins. Specifichigh-affinity IgG antibodies directed to the surface of target cells“arm” the cytotoxic cells and are absolutely required for such killing.Lysis of the target cell is extracellular, requires direct cell-to-cellcontact, and does not involve complement. It is contemplated that, inaddition to antibodies, other proteins comprising Fc regions,specifically Fc fusion proteins, having the capacity to bindspecifically to an antigen-bearing target cell will be able to effectcell-mediated cytotoxicity. For simplicity, the cell-mediatedcytotoxicity resulting from the activity of an Fc fusion protein is alsoreferred to herein as ADCC activity.

A polypeptide, antibody, polynucleotide, vector, cell, or compositionwhich is “isolated” is a polypeptide, antibody, polynucleotide, vector,cell, or composition which is in a form not found in nature. Isolatedpolypeptides, antibodies, polynucleotides, vectors, cells orcompositions include those which have been purified to a degree thatthey are no longer in a form in which they are found in nature. In someaspects, an antibody, polynucleotide, vector, cell, or composition whichis isolated is substantially pure.

The term “subject” refers to any animal (e.g., a mammal), including, butnot limited to humans, non-human primates, rodents, and the like, whichis to be the recipient of a particular treatment. Typically, the terms“subject” and “patient” are used interchangeably herein in reference toa human subject.

The term “pharmaceutical composition” refers to a preparation which isin such form as to permit the biological activity of the activeingredient (e.g., an anti-CD73 binding molecule disclosed herein) to beeffective, and which contains no additional components which areunacceptably toxic to a subject to which the composition would beadministered. Such composition can be sterile.

An “effective amount” of an anti-CD73 binding molecule as disclosedherein is an amount sufficient to carry out a specifically statedpurpose. An “effective amount” can be determined empirically and in aroutine manner, in relation to the stated purpose.

The term “therapeutically effective amount” refers to an amount of ananti-CD73 binding molecule disclosed herein or other drug effective to“treat” a disease or disorder in a subject or mammal.

The word “label” when used herein refers to a detectable compound orcomposition which is fused (e.g., genetically fused) or conjugated(e.g., chemically conjugated) directly or indirectly to an anti-CD73binding molecule disclosed herein so as to generate a “labeled”anti-CD73 binding molecule. The label can be detectable by itself (e.g.,radioisotope labels or fluorescent labels) or, in the case of anenzymatic label, can catalyze chemical alteration of a substratecompound or composition which is detectable.

Terms such as “derivatizable group” and “derivatizable functional group”are used interchangeably and refer to a functional group that is capableof reacting to permit the formation of a covalent bond between ananti-CD73 binding molecule disclosed herein (e.g., a CD73 antibody) andanother substance. In some aspects, such substance is a therapeuticagent (e.g., a cytotoxin), a detectable label, a polymer (e.g., PEG),etc. Exemplary derivatizable groups include thiol, hydroxyl, amino,carboxy, and amide, as well as modified forms thereof, such as activatedor protected forms.

Terms such as “treating” or “treatment” or “to treat” or “alleviating”or “to alleviate” refer to both (1) therapeutic measures that cure, slowdown, lessen symptoms of, and/or halt progression of a diagnosedpathologic condition or disorder and (2) prophylactic or preventativemeasures that prevent and/or slow the development of a targetedpathologic condition or disorder. Thus, those in need of treatmentinclude those already with the disorder; those prone to have thedisorder; and those in whom the disorder is to be prevented. In certainaspects, a subject is successfully “treated” for cancer according to themethods of the present disclosure if the patient shows, e.g., total,partial, or transient remission of a certain type of cancer.

The terms “cancer”, “tumor”, “cancerous”, and “malignant” refer to ordescribe the physiological condition in mammals that is typicallycharacterized by unregulated cell growth. Examples of cancers includebut are not limited to, lymphomas, non-small cell lung cancer, Hodgkin'sand non-Hodgkin's lymphoma, breast cancer (including hormonally mediatedbreast cancer, see, e.g., Innes et al. (2006) Br. J. Cancer94:1057-1065), colon cancer, In some aspects, the term cancer as usedherein specifically refers to cancer expressing CD73 (e.g., coloncancer, breast cancer, lymphoma, non-small cell carcinoma).

“Polynucleotide,” or “nucleic acid,” as used interchangeably herein,refer to polymers of nucleotides of any length, and include DNA and RNA.The nucleotides can be deoxyribonucleotides, ribonucleotides, modifiednucleotides or bases, and/or their analogs, or any substrate that can beincorporated into a polymer by DNA or RNA polymerase. A polynucleotidecan comprise modified nucleotides, such as methylated nucleotides andtheir analogs. The preceding description applies to all polynucleotidesreferred to herein, including RNA and DNA.

The term “vector” means a construct, which is capable of delivering, andin some aspects, expressing, one or more gene(s) or sequence(s) ofinterest in a host cell. Examples of vectors include, but are notlimited to, viral vectors, naked DNA or RNA expression vectors, plasmid,cosmid or phage vectors, DNA or RNA expression vectors associated withcationic condensing agents, DNA or RNA expression vectors encapsulatedin liposomes, and certain eukaryotic cells, such as producer cells.

The terms “polypeptide,” “peptide,” and “protein” are usedinterchangeably herein to refer to polymers of amino acids of anylength. The polymer can be linear or branched, it can comprise modifiedamino acids, and it can be interrupted by non-amino acids. The termsalso encompass an amino acid polymer that has been modified naturally orby intervention; for example, disulfide bond formation, glycosylation,lipidation, acetylation, phosphorylation, or any other manipulation ormodification, such as conjugation with a labeling component. Alsoincluded within the definition are, for example, polypeptides containingone or more analogs of an amino acid (including, for example, unnaturalamino acids, etc.), as well as other modifications known in the art. Itis understood that, because the polypeptides of the instant disclosureare based upon antibodies, in certain aspects, the polypeptides canoccur as single chains or associated chains.

A “recombinant” polypeptide or protein refers to a polypeptide orprotein produced via recombinant DNA technology. Recombinantly producedpolypeptides and proteins expressed in engineered host cells areconsidered isolated, as are native or recombinant polypeptides whichhave been separated, fractionated, or partially or substantiallypurified by any suitable technique. The polypeptides disclosed hereincan be recombinantly produced using methods known in the art.Alternatively, the proteins and peptides disclosed herein can bechemically synthesized.

The term “amino acid substitution” refers to replacing an amino acidresidue present in a parent sequence with another amino acid residue. Anamino acid can be substituted in a parent sequence, for example, viachemical peptide synthesis or through recombinant methods known in theart. Accordingly, references to a “substitution at position X” or“substitution at position X” refer to the substitution of an amino acidpresent at position X with an alternative amino acid residue. In someaspects, substitution patterns can described according to the schemaAXY, wherein A is the single letter code corresponding to the amino acidnaturally present at position X, and Y is the substituting amino acidresidue. In other aspects, substitution patterns can described accordingto the schema XY, wherein Y is the single letter code corresponding tothe amino acid residue substituting the amino acid naturally present atposition X.

A “conservative amino acid substitution” is one in which the amino acidresidue is replaced with an amino acid residue having a similar sidechain. Families of amino acid residues having similar side chains havebeen defined in the art, including basic side chains (e.g., lysine,arginine, histidine), acidic side chains (e.g., aspartic acid, glutamicacid), uncharged polar side chains (e.g., glycine, asparagine,glutamine, serine, threonine, tyrosine, cysteine), nonpolar side chains(e.g., alanine, valine, leucine, isoleucine, proline, phenylalanine,methionine, tryptophan), beta-branched side chains (e.g., threonine,valine, isoleucine) and aromatic side chains (e.g., tyrosine,phenylalanine, tryptophan, histidine). Thus, if an amino acid in apolypeptide is replaced with another amino acid from the same side chainfamily, the substitution is considered to be conservative. In anotheraspect, a string of amino acids can be conservatively replaced with astructurally similar string that differs in order and/or composition ofside chain family members.

Non-conservative substitutions include those in which (i) a residuehaving an electropositive side chain (e.g., Arg, His or Lys) issubstituted for, or by, an electronegative residue (e.g., Glu or Asp),(ii) a hydrophilic residue (e.g., Ser or Thr) is substituted for, or by,a hydrophobic residue (e.g., Ala, Leu, Ile, Phe or Val), (iii) acysteine or proline is substituted for, or by, any other residue, or(iv) a residue having a bulky hydrophobic or aromatic side chain (e.g.,Val, His, Ile or Trp) is substituted for, or by, one having a smallerside chain (e.g., Ala, Ser) or no side chain (e.g., Gly).

Other substitutions can be readily identified by workers of ordinaryskill. For example, for the amino acid alanine, a substitution can betaken from any one of D-alanine, glycine, beta-alanine, L-cysteine andD-cysteine. For lysine, a replacement can be any one of D-lysine,arginine, D-arginine, homo-arginine, methionine, D-methionine, omithine,or D-ornithine. Generally, substitutions in functionally importantregions that can be expected to induce changes in the properties ofisolated polypeptides are those in which (i) a polar residue, e.g.,serine or threonine, is substituted for (or by) a hydrophobic residue,e.g., leucine, isoleucine, phenylalanine, or alanine; (ii) a cysteineresidue is substituted for (or by) any other residue; (iii) a residuehaving an electropositive side chain, e.g., lysine, arginine orhistidine, is substituted for (or by) a residue having anelectronegative side chain, e.g., glutamic acid or aspartic acid; or(iv) a residue having a bulky side chain, e.g., phenylalanine, issubstituted for (or by) one not having such a side chain, e.g., glycine.The likelihood that one of the foregoing non-conservative substitutionscan alter functional properties of the protein is also correlated to theposition of the substitution with respect to functionally importantregions of the protein: some non-conservative substitutions canaccordingly have little or no effect on biological properties.

The term “amino acid insertion” refers to introducing a new amino acidresidue between two amino acid residues present in the parent sequence.An amino acid can be inserted in a parent sequence, for example, viachemical peptide synthesis or through recombinant methods known in theart. Accordingly as used herein, the phrases “insertion betweenpositions X and Y” or “insertion between Kabat positions X and Y,”wherein X and Y correspond to amino acid positions (e.g., a cysteineamino acid insertion between positions 239 and 240), refers to theinsertion of an amino acid between the X and Y positions, and also tothe insertion in a nucleic acid sequence of a codon encoding an aminoacid between the codons encoding the amino acids at positions X and Y.Insertion patterns can be described according to the schema AXins,wherein A is the single letter code corresponding to the amino acidbeing inserted, and X is the position preceding the insertion.

The term “percent sequence identity” between two polypeptide orpolynucleotide sequences refers to the number of identical matchedpositions shared by the sequences over a comparison window, taking intoaccount additions or deletions (i.e., gaps) that must be introduced foroptimal alignment of the two sequences. A matched position is anyposition where an identical nucleotide or amino acid is presented inboth the target and reference sequence. Gaps presented in the targetsequence are not counted since gaps are not nucleotides or amino acids.Likewise, gaps presented in the reference sequence are not counted sincetarget sequence nucleotides or amino acids are counted, not nucleotidesor amino acids from the reference sequence.

The percentage of sequence identity is calculated by determining thenumber of positions at which the identical amino-acid residue or nucleicacid base occurs in both sequences to yield the number of matchedpositions, dividing the number of matched positions by the total numberof positions in the window of comparison and multiplying the result by100 to yield the percentage of sequence identity. The comparison ofsequences and determination of percent sequence identity between twosequences can be accomplished using readily available software both foronline use and for download. Suitable software programs are availablefrom various sources, and for alignment of both protein and nucleotidesequences. One suitable program to determine percent sequence identityis bl2seq, part of the BLAST suite of program available from the U.S.government's National Center for Biotechnology Information BLAST website (blast.ncbi.nlm.nih.gov). Bl2seq performs a comparison between twosequences using either the BLASTN or BLASTP algorithm. BLASTN is used tocompare nucleic acid sequences, while BLASTP is used to compare aminoacid sequences. Other suitable programs are, e.g., Needle, Stretcher,Water, or Matcher, part of the EMBOSS suite of bioinformatics programsand also available from the European Bioinformatics Institute (EBI) atwww.ebi.ac.uk/Tools/psa.

Different regions within a single polynucleotide or polypeptide targetsequence that aligns with a polynucleotide or polypeptide referencesequence can each have their own percent sequence identity. It is notedthat the percent sequence identity value is rounded to the nearesttenth. For example, 80.11, 80.12, 80.13, and 80.14 are rounded down to80.1, while 80.15, 80.16, 80.17, 80.18, and 80.19 are rounded up to80.2. It also is noted that the length value will always be an integer.

In certain aspects, the percentage identity “X” of a first amino acidsequence to a second sequence amino acid is calculated as 100×(Y/Z),where Y is the number of amino acid residues scored as identical matchesin the alignment of the first and second sequences (as aligned by visualinspection or a particular sequence alignment program) and Z is thetotal number of residues in the second sequence. If the length of afirst sequence is longer than the second sequence, the percent identityof the first sequence to the second sequence will be higher than thepercent identity of the second sequence to the first sequence.

One skilled in the art will appreciate that the generation of a sequencealignment for the calculation of a percent sequence identity is notlimited to binary sequence-sequence comparisons exclusively driven byprimary sequence data. Sequence alignments can be derived from multiplesequence alignments. One suitable program to generate multiple sequencealignments is ClustalW2, available from www.clustal.org. Anothersuitable program is MUSCLE, available from www.drive5.com/muscle/.ClustalW2 and MUSCLE are alternatively available, e.g., from the EBI.

It will also be appreciated that sequence alignments can be generated byintegrating sequence data with data from heterogeneous sources such asstructural data (e.g., crystallographic protein structures), functionaldata (e.g., location of mutations), or phylogenetic data. A suitableprogram that integrates heterogeneous data to generate a multiplesequence alignment is T-Coffee, available at www.tcoffee.org, andalternatively available, e.g., from the EBI. It will also be appreciatedthat the final alignment used to calculate percent sequence identity canbe curated either automatically or manually.

The term “consensus sequence,” as used herein with respect to lightchain (VL) and heavy chain (VH) variable regions, refers to a compositeor genericized VL or VH sequence defined based on information as towhich amino acid residues within the VL or VH chain are amenable tomodification without detriment to antigen-binding. Thus, in a “consensussequence” for a VL or VH chain, certain amino acid positions areoccupied by one of multiple possible amino acid residues at thatposition. For example, if an arginine (R) or a serine (S) occur at aparticular position, then that particular position within the consensussequence can be either arginine or serine (R or S). Consensus sequencesfor VH and VL chain can be defined, for example, by in vitro affinitymaturation (e.g., randomizing every amino acid position in a certain CDRusing degenerate coding primers), by scanning mutagenesis (e.g., alaninescanning mutagenesis) of amino acid residues within the antibody CDRs,or any other methods known in the art, followed by evaluation of thebinding of the mutants to the antigen to determine whether the mutatedamino acid position affects antigen-binding. In some aspects, mutationsare introduced in the CDR regions. In other aspects, mutations areintroduced in framework regions. In some other aspects, mutations areintroduced in CDR and framework regions.

II. CD73-BINDING MOLECULES

The present disclosure provides CD73 binding molecules, e.g., antibodiesand antigen-binding fragments thereof that specifically bind CD73, forexample, human CD73. The full-length amino acid (aa) and nucleotide (nt)sequences for CD73 are known in the art (see, e.g., UniProt Acc. No.P21589 for human CD73, or UniProt Acc. No. Q61503 for mouse CD73). Insome aspects, the anti-CD73 binding molecules are human antibodies (forexample, a clone 10.3 antibody, a clone 2C5 antibody, MEDI9447). Incertain aspects, the CD73 binding molecules are antibodies orantigen-binding fragments thereof.

In some aspects, CD73 binding molecules, e.g., antibodies orantigen-binding fragments thereof comprise a Fab, a Fab′, a F(ab′)₂, aFd, a single chain Fv or scFv, a disulfide linked Fv, a V-NAR domain, anIgNar, an intrabody, an IgG CH2, a minibody, a F(ab′)₃, a tetrabody, atriabody, a diabody, a single-domain antibody, DVD-Ig, Fcab, mAb², a(scFv)₂, or a scFv-Fc. In some aspects, the antibody is of the IgG type,for example of the IgG1 type.

In some aspects, the anti-CD73 antibody (for example, MEDI9447, a clone10.3 antibody or a clone 2C5 antibody) or antigen-binding fragmentthereof comprises a heavy chain constant region or fragment thereof. Insome specific aspects, the heavy chain constant region is an IgGconstant region. The IgG constant region can comprise a light chainconstant region selected from the group consisting of a kappa constantregion and a lambda constant region.

In certain aspects, anti-CD73 antibodies or antigen-binding fragmentsthereof disclosed herein are modified compared to a parent antibody,e.g., the CD730010 antibody or the CD730002 antibody. In some aspects,the parent antibody is CD730010. In other aspects, the parent antibodyis CD730002. In other aspects, the parent antibody is CD730004,CD730008, CD7300011, CD730021, CD730042, CD730046, CD730047, CD730068,or CD730069. The modifications can include mutations in the CDR regionsand/or in the FW regions as compared to the parent antibody, e.g.,CD730010 or CD730002.

The phrase “CD730002 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:1 and two VHdomains comprising the amino acid sequence of SEQ ID NO: 2.

The phrase “CD730004 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:104 and two VHdomains comprising the amino acid sequence of SEQ ID NO:103.

The phrase “CD730008 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:106 and two VHdomains comprising the amino acid sequence of SEQ ID NO: 107.

The phrase “CD730010 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:3 and two VHdomains comprising the amino acid sequence of SEQ ID NO: 4.

The phrase “CD730011 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:5 and two VHdomains comprising the amino acid sequence of SEQ ID NO: 6.

The phrase “CD730021 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:7 and two VHdomains comprising the amino acid sequence of SEQ ID NO: 8.

The phrase “CD730042 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:9 and two VHdomains comprising the amino acid sequence of SEQ ID NO: 10.

The phrase “CD730046 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:11 and two VHdomains comprising the amino acid sequence of SEQ ID NO:12.

The phrase “CD730047 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:13 and two VHdomains comprising the amino acid sequence of SEQ ID NO:14.

The phrase “CD730068 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:108 and two VHdomains comprising the amino acid sequence of SEQ ID NO:107.

The phrase “CD730069 antibody” refers to an IgG1 comprising two VLdomains comprising the amino acid sequence of SEQ ID NO:110 and two VHdomains comprising the amino acid sequence of SEQ ID NO:109.

(i) CD730010-Derived Anti-CD73 Antibodies

In certain aspects, an anti-CD73 antibody of the present disclosurecomprises modifications to CDR1 and/or CDR2 and/or CDR3 of the lightchain of the CD730010 antibody, including, but not limited to:

1) a light chain CDR1 comprising the consensus sequence SGSLSNIGRNX₁VN(SEQ ID NO: 132), wherein X₁ represents amino acid residues Proline (P),Glutamic Acid (E) or Aspartic Acid (D); and/or,

2) a light chain CDR2 comprising the consensus sequence LX₂NX₃RX₄X₅ (SEQID NO: 133), wherein X₂ represents amino acid residues Asparagine (N) orAspartic Acid (D), X₃ represents amino acid residues Glutamine (Q) orLeucine (L), X₄ represents amino acid residues Leucine (L) or Proline(P), and X₅ represents amino acid residues Glycine (G) or Serine (S);and/or,

3) a light chain CDR3 comprising the consensus sequence ATWDDSX₆X₇GWX₈(SEQ ID NO: 134), wherein X₆ represents amino acid residues Leucine (L)or Histidine (H), X₇ represents amino acid residues Lysine (K), Proline(P), Isoleucine (I) or Asparagine (N), and X₈ represents amino acidresidues Leucine (L) or Threonine (T).

In certain aspects, an anti-CD73 antibody of the present disclosurecomprises modifications to CDR1 and/or CDR2 and/or CDR3 of the heavychain of the CD730010 antibody, including, but not limited to:

1) a heavy chain CDR1 comprising the consensus sequence SYAX₉S (SEQ IDNO: 135), wherein X₉ represents amino acid residues Methionine (M) orTyrosine (Y); and/or,

2) a heavy chain CDR2 comprising the consensus sequenceX₁₀IX₁₁GSX₁₂GX₁₃TYYADSVKG (SEQ ID NO: 136), wherein X₁₀ represents aminoacid residues Leucine (L) or Alanine (A), X_(ii) represents amino acidresidues Tryptophan (W) or Serine (S), X₁₂ represents amino acidresidues Tryptophan (W) or Glycine (G), and X₁₃ represents amino acidresidues Serine (S) or Arginine (R); and/or,

3) a heavy chain CDR3 comprising the consensus sequence LGYX₁₄X₁₅X₁₆DX₁₇(SEQ ID NO: 137), wherein X₁₄ represents amino acid residues Glycine (G)or Serine (S), X₁₅ represents amino acid residues Arginine (R) orThreonine (T), X₁₆ represents amino acid residues Valine (V) orIsoleucine (I), and X₁₇ represents amino acid residues Tyrosine (Y),Lysine (K), Methionine (M), Leucine (L) or Glutamic acid (E).

In one aspect, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL region comprising the consensus amino acidsequence:

(SEQ ID NO: 138) [FW₁]SGSLSNIGRNX₁VN[FW₂] LX₂NX₃RX₄X₅[FW₃]ATWDDSX₆X₇GWX₈[FW₄]wherein [FW₁], [FW₂], [FW₃] and [FW₄] represent the amino acid residuesof VL framework region 1 (SEQ ID NO: 25 or 26), VL framework region 2(SEQ ID NO: 27 or 28), VL framework region 3 (SEQ ID NO: 29) and VLframework region 4 (SEQ ID NO: 30), respectively, and whereinX₁ represents amino acid residues Proline (P), Glutamic Acid (E) orAspartic Acid (D);X₂ represents amino acid residues Asparagine (N) or Aspartic Acid (D);X₃ represents amino acid residues Glutamine (Q) or Leucine (L);X₄ represents amino acid residues Leucine (L) or Proline (P);X₅ represents amino acid residues Glycine (G) or Serine (S);X₆ represents amino acid residues Leucine (L) or Histidine (H);X₇ represents amino acid residues Lysine (K), Proline (P), Isoleucine(I) or Asparagine (N); and,X₈ represents amino acid residues Leucine (L) or Threonine (T).

In one aspect, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH region which comprises the consensus amino acidsequence:

(SEQ ID NO: 139) [FW₅]SYAX₉S [FW₆]X₁₀IX₁₁GSX₁₂GX₁₃TYYADSVKG[FW₇]LGYX₁₄X₁₅X₁₆DX₁₇ [FW₈]wherein [FW₅], [FW₆], [FW_(D)] and [FW₈] represent the amino acidresidues of VH framework region 1 (SEQ ID NO: 31), VH framework region 2(SEQ ID NO: 32), VH framework region 3 (SEQ ID NO: 33) and VH frameworkregion 4 (SEQ ID NO: 34), respectively, and whereinX₉ represents amino acid residues Methionine (M) or Tyrosine (Y);X₁₀ represents amino acid residues Leucine (L) or Alanine (A);X₁₁ represents amino acid residues Tryptophan (W) or Serine (S);X₁₂ represents amino acid residues Tryptophan (W) or Glycine (G);X₁₃ represents amino acid residues Serine (S) or Arginine (R);X₁₄ represents amino acid residues Glycine (G) or Serine (S);X₁₅ represents amino acid residues Arginine (R) or Threonine (T);X₁₆ represents amino acid residues Valine (V) or Isoleucine (I)X₁₇ represents amino acid residues Tyrosine (Y), Lysine (K), Methionine(M), Leucine (L) or Glutamic acid (E).

In one aspect, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL region comprising the consensus amino acidsequence:

(SEQ ID NO: 138) [FW₁]SGSLSNIGRNX₁VN[FW₂] LX₂NX₃RX₄X₅[FW₃]ATWDDSX₆X₇GWX₈[FW₄]wherein [FW₁], [FW₂], [FW₃] and [FW₄] represent the amino acid residuesof VL framework region 1 (SEQ ID NO: 25 or 26), VL framework region 2(SEQ ID NO: 27 or 28), VL framework region 3 (SEQ ID NO: 29) and VLframework region 4 (SEQ ID NO: 30), respectively, and whereinX₁ represents amino acid residues Proline (P), Glutamic Acid (E) orAspartic Acid (D);X₂ represents amino acid residues Asparagine (N) or Aspartic Acid (D);X₃ represents amino acid residues Glutamine (Q) or Leucine (L);X₄ represents amino acid residues Leucine (L) or Proline (P);X₅ represents amino acid residues Glycine (G) or Serine (S);X₆ represents amino acid residues Leucine (L) or Histidine (H);X₇ represents amino acid residues Lysine (K), Proline (P), Isoleucine(I) or Asparagine (N); and,X₈ represents amino acid residues Leucine (L) or Threonine (T);and wherein the anti-CD73 antibody or antigen-binding fragment thereoffurther comprises a VH region which comprises the consensus amino acidsequence:

(SEQ ID NO: 139) [FW₅]SYAX₉S [FW₆]X₁₀IX₁₁GSX₁₂GX₁₃TYYADSVKG[FW₇]LGYX₁₄X₁₅X₁₆DX₁₇ [FW₈]wherein [FW₅], [FW₆], [FW_(D)] and [FW₈] represent the amino acidresidues of VH framework region 1 (SEQ ID NO: 31), VH framework region 2(SEQ ID NO: 32), VH framework region 3 (SEQ ID NO: 33) and VH frameworkregion 4 (SEQ ID NO: 34), respectively, and whereinX₉ represents amino acid residues Methionine (M) or Tyrosine (Y);X₁₀ represents amino acid residues Leucine (L) or Alanine (A);X₁₁ represents amino acid residues Tryptophan (W) or Serine (S);X₁₂ represents amino acid residues Tryptophan (W) or Glycine (G);X₁₃ represents amino acid residues Serine (S) or Arginine (R);X₁₄ represents amino acid residues Glycine (G) or Serine (S);X₁₅ represents amino acid residues Arginine (R) or Threonine (T);X₁₆ represents amino acid residues Valine (V) or Isoleucine (I)X₁₇ represents amino acid residues Tyrosine (Y), Lysine (K), Methionine(M), Leucine (L) or Glutamic acid (E).

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 46, 47, and 48. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR1 comprising a sequence selected from the group consisting of SEQID NOs: 46, 47, and 48.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 49, 50, 51, and 52. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR2 comprising a sequence selected from the group consisting of SEQID NOs: 49, 50, 51 and 52.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR3 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 53, 54, 55, and 56. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR3 comprising a sequence selected from the group consisting of SEQID NOs: 53, 54, 55, and 56.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 35 and 36. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR1 comprising a sequence selected from the group consisting of SEQID NOs: 35 and 36.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 37, 38, 39, and 40. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR2 comprising a sequence selected from the group consisting of SEQID NOs: 37, 38, 39, and 40.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR3 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 41, 42, 43, 44, and 45. In some aspects,the anti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR3 comprising a sequence selected from the group consisting of SEQID NOs: 41, 42, 43, 44, and 45.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 46, 47, and 48, except for one, two,three or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment comprises a VL-CDR1 comprising asequence selected from the group consisting of SEQ ID NOs: 46, 47, and48, except for one, two, three or four amino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 49, 50, 51, and 52, except for one, two,three, or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VL-CDR2comprising a sequence selected from the group consisting of SEQ ID NOs:49, 50, 51, and 52, except for one, two, three or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR3 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 53, 54, 55, and 56, except for one, two,three, or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VL-CDR3comprising a sequence selected from the group consisting of SEQ ID NOs:53, 54, 55, and 56, except for one, two, three or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 35 and 36, except for one, two, three,or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VH-CDR1comprising a sequence selected from the group consisting of SEQ ID NOs:35 and 36, except for one, two, three or four amino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 37, 38, 39, and 40, except for one, two,three, or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VH-CDR2comprising a sequence selected from the group consisting of SEQ ID NOs:37, 38, 39, and 40, except for one, two, three or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR3 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 41, 42, 43, 44, and 45, except for one,two, three, or four amino acid substitutions. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR3 comprising sequence selected from the group consisting of SEQ IDNOs: 41, 42, 43, 44, and 45, except for one, two, three or four aminoacid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 46, 47 and 48; a VL-CDR2 consisting of asequence selected from the group consisting of SEQ ID NOs: 49, 50, 51,and 52; and a VL-CDR3 consisting of a sequence selected from the groupconsisting of SEQ ID NOs: 53, 54, 55, and 56. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR1 comprising a sequence selected from the group consisting of SEQID NOs: 46, 47 and 48; a VL-CDR2 comprising a sequence selected from thegroup consisting of SEQ ID NOs: 49, 50, 51, and 52; and a VL-CDR3comprising a sequence selected from the group consisting of SEQ ID NOs:53, 54, 55, and 56.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 35 and 36; a VH-CDR2 consisting of asequence selected from the group consisting of SEQ ID NOs: 37, 38, 39,and 40; and a VH-CDR3 consisting of a sequence selected from the groupconsisting of SEQ ID NOs: 41, 42, 43, 44, and 45. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR1 comprising a sequence selected from the group consisting of SEQID NOs: 35 and 36; a VH-CDR2 comprising a sequence selected from thegroup consisting of SEQ ID NOs: 37, 38, 39, and 40; a VH-CDR3 comprisinga sequence selected from the group consisting of SEQ ID NOs: 41, 42, 43,44, and 45.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 46, 47 and 48 except for one, two, threeor four amino acid substitutions; a VL-CDR2 consisting of a sequenceselected from the group consisting of SEQ ID NOs: 49, 50, 51, and 52except for one, two, three or four amino acid substitutions; and aVL-CDR3 consisting of a sequence selected from the group consisting ofSEQ ID NOs: 53, 54, 55, and 56 except for one, two, three or four aminoacid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 comprising a sequence selected from thegroup consisting of SEQ ID NOs: 46, 47 and 48 except for one, two,three, or four amino acid substitutions; a VL-CDR2 comprising a sequenceselected from the group consisting of SEQ ID NOs: 49, 50, 51, and 52except for one, two, three, or four amino acid substitutions; and aVL-CDR3 comprising a sequence selected from the group consisting of SEQID NOs: 53, 54, 55, and 56 except for one, two, three or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 35 and 36 except for one, two, three, orfour amino acid substitutions; a VH-CDR2 consisting of a sequenceselected from the group consisting of SEQ ID NOs: 37, 38, 39, and 40except for one, two, three, or four amino acid substitutions; and aVH-CDR3 consisting of a sequence selected from the group consisting ofSEQ ID NOs: 41, 42, 43, 44, and 45 except for one, two, three or fouramino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 comprising a sequence selected from thegroup consisting of SEQ ID NOs: 35 and 36 except for one, two, three, orfour amino acid substitutions; a VH-CDR2 comprising a sequence selectedfrom the group consisting of SEQ ID NOs: 37, 38, 39, and 40 except forone, two, three, or four amino acid substitutions; a VH-CDR3 comprisinga sequence selected from the group consisting of SEQ ID NOs: 41, 42, 43,44, and 45 except for one, two, three or four amino acid substitutions.

In certain aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises modifications to CDR1, and/or CDR2, and/or CDR3 of theheavy and/or light chain, and further comprises modifications to FW1,and/or FW2, and/or FW3, and/or FW4 of the heavy and/or light chain.

In some aspects, FW₁ comprises SEQ ID NO: 25 or 26, FW₂ comprises SEQ IDNO: 27 or 28, FW₃ comprises SEQ ID NO: 29, FW₄ comprises SEQ ID NO: 30,FW₅ comprises SEQ ID NO: 31, FW₆ comprises SEQ ID NO: 32, FW₇ comprisesSEQ ID NO: 33, and FW₈ comprises SEQ ID NO: 34.

In some aspects, FW₁ comprises SEQ ID NO: 25 or 26, except for one, two,three, or four amino acid substitutions; FW₂ comprises SEQ ID NO: 27 or28, except for one, two, three, or four amino acid substitutions; FW₃comprises SEQ ID NO: 29, except for one, two, three, or four amino acidsubstitutions; FW₄ comprises SEQ ID NO: 30, except for one, two, three,or four amino acid substitutions; FW₅ comprises SEQ ID NO: 31, exceptfor one, two, three, or four amino acid substitutions; FW₆ comprises SEQID NO: 32, except for one, two, three, or four amino acid substitutions;FW₇ comprises SEQ ID NO: 33, except for one, two, three, or four aminoacid substitutions; and FW₈ comprises SEQ ID NO: 34.

In certain aspects, the anti-CD733 antibody or antigen-binding fragmentthereof comprises a VL and a VH comprising VL-CDR1, VL-CRD2, VL-CDR3,VH-CDR1, VH-CDR2, and VH-CDR3 amino acid sequences identical oridentical except for one, two, three or four amino acid substitutions inone or more CDRs, wherein such VL-CDR1, VL-CRD2, VL-CDR3, VH-CDR1,VH-CDR2, and VH-CDR3 are:

SEQ ID NOs: 46, 49, 53, 35, 37, and 41; or, SEQ ID NOs: 47, 49, 53, 35,37 and 41; or, SEQ ID NOs: 47, 49, 54, 36, 37 and 42; or, SEQ ID NOs:46, 50, 54, 36, 38 and 43; or, SEQ ID NOs: 46, 51, 55, 36, 39 and 44;or, SEQ ID NOs: 48, 52, 54, 36, 40 and 44; or, SEQ ID NOs: 46, 49, 56,35, 37 and 41; or, SEQ ID NOs: 46, 49, 53, 35, 37 and 45; or, SEQ IDNOs: 47, 49, 56, 36, 37 and 45; or, SEQ ID NOs: 46, 50, 56, 36, 38 and45; or, SEQ ID NOs: 46, 51, 56, 36, 39 and 45; or, SEQ ID NOs: 48, 52,56, 36, 40 and 45; or

SEQ ID NOs: 46, 49, 56, 35, 37 and 45, respectively.

In certain aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises an antibody VL and an antibody VH, wherein the VLcomprises an amino acid sequence at least about 80%, about 85%, about90%, about 95%, about 96%, about 97%, about 98%, about 99%, or about100% identical to a reference amino acid sequence selected from thegroup consisting of SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQ IDNO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64, SEQID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO: 69,and SEQ ID NO: 70.

In other aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises an antibody VL and an antibody VH, wherein the VHcomprises an amino acid sequence at least about 80%, about 85%, about90%, about 95%, about 96%, about 97%, about 98%, about 99%, or about100% identical to a reference amino acid sequence selected from thegroup consisting of SEQ ID NO: 71, SEQ ID NO: 72, SEQ ID NO: 73, SEQ IDNO: 74, SEQ ID NO: 75, SEQ ID NO: 76, SEQ ID NO: 77, SEQ ID NO: 78, SEQID NO: 79, SEQ ID NO: 80, SEQ ID NO: 80, SEQ ID NO: 81, SEQ ID NO: 82,SEQ ID NO: 83 and SEQ ID NO: 84.

In other aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL comprising a sequence at least about 80%, about85%, about 90%, about 95%, about 96%, about 97%, about 98%, about 99%,or about 100% identical to a reference amino acid sequence selected fromthe group consisting of SEQ ID NO: 57, SEQ ID NO: 58, SEQ ID NO: 59, SEQID NO: 60, SEQ ID NO: 61, SEQ ID NO: 62, SEQ ID NO: 63, SEQ ID NO: 64,SEQ ID NO: 65, SEQ ID NO: 66, SEQ ID NO: 67, SEQ ID NO: 68, SEQ ID NO:69, and SEQ ID NO: 70, and further comprises a VH comprising a sequenceat least about 80%, about 85%, about 90%, about 95%, about 96%, about97%, about 98%, about 99%, or about 100% identical to a reference aminoacid sequence selected from the group consisting of SEQ ID NO: 71, SEQID NO: 72, SEQ ID NO: 73, SEQ ID NO: 74, SEQ ID NO: 75, SEQ ID NO: 76,SEQ ID NO: 77, SEQ ID NO: 78, SEQ ID NO: 79, SEQ ID NO: 80, SEQ ID NO:81, SEQ ID NO: 82, SEQ ID NO: 83 and SEQ ID NO: 84.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL comprising the sequence of SEQ ID NO: 68 and a VHcomprising the sequence of SEQ ID NO:82. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VL consistingof the sequence of SEQ ID NO:68 and a VH consisting of the sequence ofSEQ ID NO:82.

The “clone 10.3 antibody” (also designated “73combo3” or “MEDI9447”) isan IgG1 comprising two CD730010-derived light chains (VL) of SEQ ID NO:68 (comprising three CDRs, CDR1, CDR2, and CDR3, with the sequences ofSEQ ID NO: 46, 51 and 56, respectively), and two CD730010-derived heavychains (VH) of SEQ ID NO: 82 (comprising three CDRs, CDR1, CDR2, andCDR3, with the sequences of SEQ ID NO: 36, 39, and 45, respectively).

In certain aspects, an anti-CD73 antibody or antigen-binding fragmentthereof disclosed herein binds CD73 with substantially the same orbetter affinity as a 10.3 antibody comprising the 10.3 heavy chain VH ofSEQ ID NO: 82 and the 10.3 light chain VL of SEQ ID NO: 68.

(ii) CD730002-Derived Anti-CD73 Antibodies

In certain aspects, the anti-CD73 antibody of the present disclosurecomprises modifications to CDR1 and/or CDR2 and/or CDR3 of the lightchain of the CD730002 antibody, including, but not limited to:

1) a light chain CDR1 comprising the sequence SGDKVGDKYAS (SEQ ID NO:97); and/or,

2) a light chain CDR2 comprising the consensus sequence EDX₁₈KX₁₉X₂₀5(SEQ ID NO: 140), wherein X₁₈ represents amino acid residues Serine (S)or Threonine (T), X₁₉ represents amino acid residues Arginine (R) orTyrosine (Y), and X₂₀ represents amino acid residues Histidine (H),Proline (P) or Leucine (L); and/or,

3) a light chain CDR3 comprising the sequence QAWDTSFWV (SEQ ID NO:100).

In certain aspects, the anti-CD73 antibody of the present disclosurecomprises modifications to CDR1 and/or CDR2 and/or CDR3 of the heavychain of CD730002, including, but not limited to:

1) a heavy chain CDR1 comprising the sequence SX₂₁A X₂₂5 (SEQ ID NO:141), wherein X₂₁ represents amino acid residues Tyrosine (Y) or Valine(V), and X₂₂ represents amino acid residues Methionine (M) or Arginine(R); and/or,

2) a heavy chain CDR2 comprising the sequence AISGSGGSX₂₃YY X₂₄DSVKX₂₅(SEQ ID NO: 142), wherein X₂₃ represents amino acid residues Threonine(T) or Proline (P); X₂₄ represents amino acid residues Alanine (A) or G(Glycine); and X₂₅ represents amino acid residues Glycine (G) orArginine (R); and/or,

3) a heavy chain CDR3 comprising the sequence DKGYYWYM (SEQ ID NO: 143).

In one aspect, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL region comprising the consensus amino acidsequence:

(SEQ ID NO: 144) [FW₉]SGDKVGDKYAS[FW₁₀]EDX₁₈KX₁₉X₂₀S[FW₁₁]QAWDTSFWV[FW₁₂]wherein [FW₉], [FW₁₀], [FW₁₁] and [FW₁₂] represent the amino acidresidues of VL framework region 1 (SEQ ID NO: 90 or 91), VL frameworkregion 2 (SEQ ID NO: 92), VL framework region 3 (SEQ ID NO: 93, 94 or122) and VL framework region 4 (SEQ ID NO: 30), respectively; andwherein X₁₈ represents amino acid residues Proline (P) or Leucine (L);X₁₉ represents amino acid residues Arginine (R) or Tyrosine (Y); and X₂₀represents amino acid residues Histidine (H), Proline (P) or Leucine(L).

In one aspect, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH region which comprises the consensus amino acidsequence:

(SEQ ID NO: 145) [FW₁₃] SX₂₁A X₂₂S[FW₁₄]AISGSGGSX₂₃YYX₂₄DSVKX₂₅[FW₁₅]DKGYYWYM[FW₁₆]wherein [FW₁₃], [FW₁₄], [FW₁₅] and [FW₁₆] represent the amino acidresidues of VH framework region 1 (SEQ ID NO: 31), VH framework region 2(SEQ ID NO: 32), VH framework region 3 (SEQ ID NO: 33) and VH frameworkregion 4 (SEQ ID NO: 89), respectively; and wherein X₂₁ represents aminoacid residues Tyrosine (Y) or Valine (V); X₂₂ represents amino acidresidues Methionine (M) or Arginine (R); X₂₃ represents amino acidresidues Threonine (T) or Proline (P); X₂₄ represents amino acidresidues Alanine (A) or G (Glycine); and X₂₅ represents amino acidresidues Glycine (G) or Arginine (R).

In one aspect, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL region comprising the consensus amino acidsequence:

(SEQ ID NO: 144) [FW₉]SGDKVGDKYAS[FW₁₀]EDX₁₈KX₁₉X₂₀S[FW₁₁]QAWDTSFWV[FW₁₂]wherein [FW₉], [FW₁₀], [FW₁₁] and [FW₁₂] represent the amino acidresidues of VL framework region 1 (SEQ ID NO: 90 or 91), VL frameworkregion 2 (SEQ ID NO: 92), VL framework region 3 (SEQ ID NO: 93, 94 or122) and VL framework region 4 (SEQ ID NO: 30), respectively; andwherein X₁₈ represents amino acid residues Proline (P) or Leucine (L);X₁₉ represents amino acid residues Arginine (R) or Tyrosine (Y); and X₂₀represents amino acid residues Histidine (H), Proline (P) or Leucine(L),and wherein the anti-CD73 antibody or antigen-binding fragment thereoffurther comprises a VH region which comprises the consensus amino acidsequence:

(SEQ ID NO: 145) [FW₁₃] SX₂₁A X₂₂S[FW₁₄]AISGSGGSX₂₃YYX₂₄DSVKX₂₅[FW₁₅]DKGYYWYM[FW₁₆]wherein [FW₁₃], [FW₁₄], [FW₁₅] and [FW₁₆] represent the amino acidresidues of VH framework region 1 (SEQ ID NO: 31), VH framework region 2(SEQ ID NO: 32), VH framework region 3 (SEQ ID NO: 33) and VH frameworkregion 4 (SEQ ID NO: 89), respectively; and wherein X₂₁ represents aminoacid residues Tyrosine (Y) or Valine (V); X₂₂ represents amino acidresidues Methionine (M) or Arginine (R); X₂₃ represents amino acidresidues Threonine (T) or Proline (P); X₂₄ represents amino acidresidues Alanine (A) or G (Glycine); and X₂₅ represents amino acidresidues Glycine (G) or Arginine (R).

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence consisting of SEQID NO: 97. In some aspects, the anti-CD73 antibody or antigen-bindingfragment thereof comprises a VL-CDR1 comprising a sequence consisting ofSEQ ID NO: 97.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 98, 99, 127, 128, and 129. In someaspects, the anti-CD73 antibody or antigen-binding fragment thereofcomprises a VL-CDR2 comprising a sequence selected from the groupconsisting of SEQ ID NOs: 98, 99, 127, 128 and 129.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR3 consisting of a sequence consisting of SEQID NO: 100. In some aspects, the anti-CD73 antibody or antigen-bindingfragment thereof comprises a VL-CDR3 comprising a sequence consisting ofSEQ ID NO: 100.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence of a sequenceselected from the group consisting of SEQ ID NOs: 35, 123 and 124. Insome aspects, the anti-CD73 antibody or antigen-binding fragment thereofcomprises a VH-CDR1 comprising a sequence selected from the groupconsisting of SEQ ID NOs: 35, 123 and 124.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 37, 95, 125 and 126. In some aspects,the anti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR2 comprising a sequence selected from the group consisting of SEQID NOs: 37, 95, 125, and 126.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR3 consisting of a sequence consisting of SEQID NO: 96. In some aspects, the anti-CD73 antibody or antigen-bindingfragment thereof comprises a VH-CDR3 comprising a sequence consisting ofSEQ ID NO: 96.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence consisting of SEQID NO: 97, except for one, two, three, or four amino acid substitutions.In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 comprising a sequence consisting of SEQ IDNO: 97, except for one, two, three or four amino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 98, 99, 127, 128, and 129, except forone, two, three, or four amino acid substitutions. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR2 comprising a sequence selected from the group consisting of SEQID NOs: 98, 99, 127, 128, and 129, except for one, two, three, or fouramino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR3 consisting of a sequence consisting of SEQID NO: 100, except for one, two, three, or four amino acidsubstitutions. In some aspects, the anti-CD73 antibody orantigen-binding fragment thereof comprises a VL-CDR3 comprising asequence consisting of SEQ ID NO: 100, except for one, two, three, orfour amino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 35, 123 and 124, except for one, two,three, or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VH-CDR1comprising a sequence selected from the group consisting of SEQ ID NOs:35, 123 and 124, except for one, two, three, or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR2 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 37, 95, 125 and 126, except for one,two, three, or four amino acid substitutions. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR2 comprising a sequence selected from the group consisting of SEQID NOs: 37, 95, 125 and 126, except for one, two, three, or four aminoacid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR3 consisting of a sequence consisting of SEQID NO: 96, except for one, two, three, or four amino acid substitutions.In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR3 comprising a sequence consisting of SEQ IDNO: 96, except for one, two, three, or four amino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence consisting of SEQID NO: 97; a VL-CDR2 consisting of a sequence selected from the groupconsisting of SEQ ID NOs: 98, 99, 127, 128, and 129; and a VL-CDR3consisting of a sequence consisting of SEQ ID NO: 100. In some aspects,the anti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR1 comprising a sequence consisting of SEQ ID NO: 97; a VL-CDR2comprising a sequence selected from the group consisting of SEQ ID NOs:98, 99, 127, 128, and 129; and a VL-CDR3 comprising a sequenceconsisting of SEQ ID NO: 100.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 35, 123, and 124; a VH-CDR2 consistingof a sequence selected from the group consisting of SEQ ID NOs: 37, 95,125, and 126; and a VH-CDR3 consisting of a sequence consisting of SEQID NOs: 96. In some aspects, the anti-CD73 antibody or antigen-bindingfragment thereof comprises a VH-CDR1 comprising a sequence selected fromthe group consisting of SEQ ID NOs: 35, 123, and 124; a VH-CDR2comprising a sequence selected from the group consisting of SEQ ID NOs:37, 95, 125, and 126; a VH-CDR3 comprising a sequence consisting of SEQID NO: 96.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 consisting of a sequence consisting of SEQID NO: 97, except for one, two, three, or four amino acid substitutions;a VL-CDR2 consisting of a sequence selected from the group consisting ofSEQ ID NOs: 98, 99, 127, 128, and 129, except for one, two, three orfour amino acid substitutions; and a VL-CDR3 consisting of a sequenceconsisting of SEQ ID NO: 100, except for one, two, three, or four aminoacid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 comprising a sequence consisting of SEQ IDNOs: 97, except for one, two, three or four amino acid substitutions; aVL-CDR2 comprising a sequence selected from the group consisting of SEQID NOs: 98, 99, 127, 128, and 129, except for one, two, three or fouramino acid substitutions; and a VL-CDR3 comprising a sequence consistingof SEQ ID NO:100, except for one, two, three or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 consisting of a sequence selected from thegroup consisting of SEQ ID NOs: 35, 123, and 124, except for one, two,three or four amino acid substitutions; a VH-CDR2 consisting of asequence selected from the group consisting of SEQ ID NOs: 37, 95, 125,and 126, except for one, two, three, or four amino acid substitutions;and a VH-CDR3 consisting of a sequence consisting of SEQ ID NO: 96,except for one, two, three or four amino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 comprising a sequence selected from thegroup consisting of SEQ ID NOs: 35, 123, and 124, except for one, two,three, or four amino acid substitutions; a VH-CDR2 comprising a sequenceselected from the group consisting of SEQ ID NOs: 37, 95, 125, and 126,except for one, two, three, or four amino acid substitutions; a VH-CDR3comprising a sequence consisting of SEQ ID NO: 96, except for one, two,three or four amino acid substitutions.

In certain aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises modifications to CDR1, and/or CDR2, and/or CDR3 of theheavy and/or light chain, and further comprises modifications to FW1,and/or FW2, and/or FW3, and/or FW4 of the heavy and/or light chain.

In some aspects, FW₉ comprises SEQ ID NO: 90 or 91, FW₁₀ comprises SEQID NO: 92, FW₁₁ comprises SEQ ID NO: 93, 94, or 122, FW₁₂ comprises SEQID NO: 30, FW₁₃ comprises SEQ ID NO: 31, FW₁₄ comprises SEQ ID NO: 32,FW₁₅ comprises SEQ ID NO: 33, and FW₁₆ comprises SEQ ID NO: 89.

In some aspects, FW₉ comprises SEQ ID NO: 90 or 91, except for one, two,three, or four amino acid substitutions, FW₁₀ comprises SEQ ID NO: 92,except for one, two, three, or four amino acid substitutions, FW_(ii)comprises SEQ ID NO: 93, 94, or 122, except for one, two, three, or fouramino acid substitutions, FW₁₂ comprises SEQ ID NO: 30, except for one,two, three, or four amino acid substitutions, FW₁₃ comprises SEQ ID NO:31, except for one, two, three, or four amino acid substitutions, FW₁₄comprises SEQ ID NO: 32, except for one, two, three, or four amino acidsubstitutions, FW₁₅ comprises SEQ ID NO: 33, except for one, two, threeor four amino acid substitutions, and FW₁₆ comprises SEQ ID NO: 89.

In certain aspects, the anti-CD733 antibody or antigen-binding fragmentthereof comprises a VL and a VH comprising VL-CDR1, VL-CRD2, VL-CDR3,VH-CDR1, VH-CDR2, and VH-CDR3 amino acid sequences identical oridentical except for one, two, three, or four amino acid substitutionsin one or more CDRs, wherein such VL-CDR1, VL-CRD2, VL-CDR3, VH-CDR1,VH-CDR2, and VH-CDR3 are:

SEQ ID NOs: 97, 98, 100, 35, 37, and 96; or, SEQ ID NOs: 97, 99, 100,35, 95 and 96; or, SEQ ID NOs: 97, 98, 100, 35, 37, and 96; or, SEQ IDNOs: 97, 99, 100, 123, 37, and 96; or, SEQ ID NOs: 97, 99, 100, 124, 37,and 96; or, SEQ ID NOs: 97, 99, 100, 35, 125, and 96; or, SEQ ID NOs:97, 99, 100, 35, 126, and 96; or, SEQ ID NOs: 97, 99, 100, 35, 95, and96; or, SEQ ID NOs: 97, 127, 100, 35, 95, and 96; or, SEQ ID NOs: 97,128, 100, 35, 95, and 96; or, SEQ ID NOs: 97, 129, 100, 35, 95, and 96;or,

SEQ ID NOs: 97, 99, 100, 35, 95, and 96; respectively.

In certain aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises an antibody VL and an antibody VH, wherein the VLcomprises an amino acid sequence at least about 80%, about 85%, about90%, about 95%, about 96%, about 97%, about 98%, about 99%, or about100% identical to a reference amino acid sequence selected from thegroup consisting of SEQ ID NOs: 86, 88, 112, 118, 119, 120, and 121.

In other aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises an antibody VL and an antibody VH, wherein the VHcomprises an amino acid sequence at least about 80%, about 85%, about90%, about 95%, about 96%, about 97%, about 98%, about 99%, or about100% identical to a reference amino acid sequence selected from thegroup consisting of SEQ ID NOs: 85, 87, 111, 113, 114, 115, 116, and117.

In other aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL comprising a sequence at least about 80%, about85%, about 90%, about 95%, about 96%, about 97%, about 98%, about 99%,or about 100% identical to a reference amino acid sequence selected fromthe group consisting of SEQ ID NOs: 86, 88, 112, 118, 119, 120, and 121;and further comprises a VH comprising a sequence at least about 80%,about 85%, about 90%, about 95%, about 96%, about 97%, about 98%, about99%, or about 100% identical to a reference amino acid sequence selectedfrom the group consisting of SEQ ID NOs: 85, 87, 111, 113, 114, 115,116, and 117.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL comprising the sequence of SEQ ID NO: 88; and aVH comprising the sequence of SEQ ID NO:87. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises a VLconsisting of the sequence of SEQ ID NO:87, and a VH consisting of thesequence of SEQ ID NO:87.

The “clone 2C5 antibody” is an IgG1 comprising two CD730002-derivedlight chains (VL) of SEQ ID NO: 88 (comprising three CDRs, CDR1, CDR2,and CDR3, with the sequences of SEQ ID NO: 97, 99, and 100,respectively), and CD7300002-derived heavy chains (VH) of SEQ ID NO: 87(comprising three CDRs, CDR1, CDR2, and CDR3, with the sequences of SEQID NO: 35, 95, and 96, respectively).

In certain aspects, an anti-CD73 antibody or antigen-binding fragmentthereof disclosed herein binds CD73 with substantially the same orbetter affinity as a 2C5 antibody comprising the 2C5 heavy chain VH ofSEQ ID NO: 87 and the 2C5 light chain VL of SEQ ID NO: 88.

(iii) Anti-CD73 Antibodies with Parent Antibodies Other than CD730002 orCD730010

In other aspects, the parent antibody of an anti-CD73 antibody orantigen-binding fragment disclosed herein is CD730004 (i.e., ananti-CD73 antibody comprising a VL of SEQ ID NO: 104 and a VH of SEQ IDNO:103), CD730008 (i.e., an anti-CD73 antibody comprising a VL of SEQ IDNO: 106 and a VH of SEQ ID NO:107), CD7300011 (i.e., an anti-CD73antibody comprising a VL of SEQ ID NO: 5 and a VH of SEQ ID NO:6),CD730021 (i.e., an anti-CD73 antibody comprising a VL of SEQ ID NO: 7and a VH of SEQ ID NO:8), CD730042 (i.e., an anti-CD73 antibodycomprising a VL of SEQ ID NO: 9 and a VH of SEQ ID NO:10), CD730046(i.e., an anti-CD73 antibody comprising a VL of SEQ ID NO: 11 and a VHof SEQ ID NO:12), CD730047 (i.e., an anti-CD73 antibody comprising a VLof SEQ ID NO: 13 and a VH of SEQ ID NO:14), CD730068 (i.e., an anti-CD73antibody comprising a VL of SEQ ID NO: 108 and a VH of SEQ ID NO:107),or CD730069 (i.e., an anti-CD73 antibody comprising a VL of SEQ ID NO:110 and a VH of SEQ ID NO:109). The modifications to the parentantibodies can include mutations in the CDR regions and/or in the FWregions as compared to the parent antibody, e.g., CD730004.

In certain aspects, the anti-CD73 antibody comprises modifications toCDR1 and/or CDR2 and/or CDR3 of the light chain of CD730004, CD730008,CD7300011, CD730021, CD730042, CD730046, CD730047, CD730068, orCD730069.

In certain aspects, the anti-CD73 antibody comprises modifications toCDR1 and/or CDR2 and/or CDR3 of the heavy chain of CD730004, CD730008,CD7300011, CD730021, CD730042, CD730046, CD730047, CD730068, orCD730069.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069. In someaspects, the anti-CD73 antibody or antigen-binding fragment thereofcomprises a VL-CDR2 from CD730004, CD730008, CD7300011, CD730021,CD730042, CD730046, CD730047, CD730068, or CD730069. In some aspects,the anti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR3 from CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069. In someaspects, the anti-CD73 antibody or antigen-binding fragment thereofcomprises a VH-CDR2 from CD730004, CD730008, CD7300011, CD730021,CD730042, CD730046, CD730047, CD730068, or CD730069. In some aspects,the anti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR3 from CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069 except forone, two, three, or four amino acid substitutions. In some aspects, theanti-CD73 antibody or antigen-binding fragment thereof comprises aVL-CDR2 from CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069, except for one, two, three,or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VL-CDR3 fromCD730004, CD730008, CD7300011, CD730021, CD730042, CD730046, CD730047,CD730068, or CD730069, except for one, two, three or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069, exceptfor one, two, three, or four amino acid substitutions. In some aspects,the anti-CD73 antibody or antigen-binding fragment thereof comprises aVH-CDR2 from CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069, except for one, two, three,or four amino acid substitutions. In some aspects, the anti-CD73antibody or antigen-binding fragment thereof comprises a VH-CDR3 fromCD730004, CD730008, CD7300011, CD730021, CD730042, CD730046, CD730047,CD730068, or CD730069, except for one, two, three or four amino acidsubstitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069; a VL-CDR2from CD730004, CD730008, CD7300011, CD730021, CD730042, CD730046,CD730047, CD730068, or CD730069; and a VL-CDR3 from CD730004, CD730008,CD7300011, CD730021, CD730042, CD730046, CD730047, CD730068, orCD730069.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069; a VH-CDR2from CD730004, CD730008, CD7300011, CD730021, CD730042, CD730046,CD730047, CD730068, or CD730069; and a VH-CDR3 from CD730004, CD730008,CD7300011, CD730021, CD730042, CD730046, CD730047, CD730068, orCD730069.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069, exceptfor one, two, three or four amino acid substitutions; a VL-CDR2 fromCD730004, CD730008, CD7300011, CD730021, CD730042, CD730046, CD730047,CD730068, or CD730069, except for one, two, three or four amino acidsubstitutions; and a VL-CDR3 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069, exceptfor one, two, three or four amino acid substitutions.

In some aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VH-CDR1 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069, exceptfor one, two, three or four amino acid substitutions; a VH-CDR2 fromCD730004, CD730008, CD7300011, CD730021, CD730042, CD730046, CD730047,CD730068, or CD730069, except for one, two, three or four amino acidsubstitutions; and a VH-CDR3 from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069, exceptfor one, two, three or four amino acid substitutions.

In certain aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises modifications to CDR1, and/or CDR2, and/or CDR3 of theheavy and/or light chain from CD730004, CD730008, CD7300011, CD730021,CD730042, CD730046, CD730047, CD730068, or CD730069, and furthercomprises modifications to FW1, and/or FW2, and/or FW3, and/or FW4 ofthe heavy and/or light chain from CD730004, CD730008, CD7300011,CD730021, CD730042, CD730046, CD730047, CD730068, or CD730069.

In certain aspects, the anti-CD733 antibody or antigen-binding fragmentthereof comprises a VL and a VH comprising VL-CDR1, VL-CRD2, VL-CDR3,VH-CDR1, VH-CDR2, and VH-CDR3 amino acid sequences identical oridentical except for one, two, three, or four amino acid substitutionsin one or more CDRs, wherein such VL-CDR1, VL-CRD2, VL-CDR3, VH-CDR1,VH-CDR2, and VH-CDR3 are from CD730004, CD730008, CD7300011, CD730021,CD730042, CD730046, CD730047, CD730068, or CD730069.

In certain aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises an antibody VL and an antibody VH, wherein the VLcomprises an amino acid sequence at least about 80%, about 85%, about90%, about 95%, about 96%, about 97%, about 98%, about 99%, or about100% identical to a reference amino acid sequence selected from VLsequences from CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069.

In other aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises an antibody VL and an antibody VH, wherein the VHcomprises an amino acid sequence at least about 80%, about 85%, about90%, about 95%, about 96%, about 97%, about 98%, about 99%, or about100% identical to a reference amino acid sequence selected from VHsequences from CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069.

In other aspects, the anti-CD73 antibody or antigen-binding fragmentthereof comprises a VL comprising a sequence at least about 80%, about85%, about 90%, about 95%, about 96%, about 97%, about 98%, about 99%,or about 100% identical to a reference amino acid sequence selected fromVL sequences from CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069, and further comprises a VHcomprising a sequence at least about 80%, about 85%, about 90%, about95%, about 96%, about 97%, about 98%, about 99%, or about 100% identicalto a reference amino acid sequence selected from VH sequences fromCD730004, CD730008, CD7300011, CD730021, CD730042, CD730046, CD730047,CD730068, or CD730069.

In certain aspects, the anti-CD73 antibody or antigen-binding fragmentthereof disclosed herein binds CD73 with substantially the same orbetter affinity as a CD730004, CD730008, CD7300011, CD730021, CD730042,CD730046, CD730047, CD730068, or CD730069 antibody.

(iv) Mixed and Matched Anti-CD73 Antibodies

The VH and VL sequences from the anti-CD73 binding molecules disclosedherein (e.g., CD730002, CD730004, CD730008, CD730010, CD730011, CD73021,CD730042, CD730046, CD730047, CD730068, or CD730069) or VH and VL ofvariants of such sequences (e.g., clone 10 GL9, clone 10 P32E, clone 10C1, clone 10 C2, clone 10 D3, clone 10 G10, clone 10 HPT, clone 10 GRVE,clone 10 combo1, clone 10 combo2, clone 10 combo3, clone 10 combo5, orclone combo6) can be “mixed and matched” to create other anti-CD73binding molecules.

In certain aspects, the VH sequences of the 10.3 antibody and the 2C5antibody are mixed and matched. In another aspect, the VL sequences ofthe 10.03 antibody and the 2C5 antibody can be mixed and matched.Additionally or alternatively, the VL and/or VH sequences of clone 10(CD730010) variants disclosed herein can be mixed and matched.Additionally or alternatively, the VL and/or VH sequences of clone 2(CD730002) variants disclosed herein can be mixed and matched.Additionally or alternatively, the VL and/or VH sequences of clone 10(CD730010) and clone 2 (CD730002) variants disclosed herein can be mixedand matched.

In some aspects, VL and/or VH mixing and matching can take place betweensequences derived from antibodies grouped in the same epitope bin (seeExample 2). As used herein, the term “epitope bin” refers to thegrouping of antibodies or antigen-binding fragments thereof that bindthe same epitope or an overlapping epitope, or compete with each otherfor binding with the same epitope or overlapping epitope. E.g.,sequences from CD730003, CD730010, CD730021, CD730042, CD730046, andCD730047, all of them antibodies belonging to “Epitope Bin B” can bemixed in matched. In other aspects, the VL and/or VH mixing and matchingcan take place between sequences derived from anti-CD73 antibodiesgrouped in different epitope bins. Accordingly, sequences fromantibodies belonging to “Epitope Bin B” can be mixed and matched withsequences from anti-CD73 antibodies in “Epitope Bin A” (CD730002,CD730004, CD730008, and CD730011) or “Epitope Bin C” (CD730068 andCD730069).

(v) Mutant Anti-CD73 Antibodies

In certain aspects, an anti-CD73 antibody (for example, MEDI9447, aclone 10.3 antibody or a clone 2C5 antibody) or antigen-binding fragmentthereof disclosed herein comprises mutations that improve the binding tohuman FcRn and improve the half-life of the anti-CD73 antibody orantigen-binding fragment thereof. In some aspects, such mutations are amethionine (M) to tyrosine (Y) mutation in position 252, a serine (S) tothreonine (T) mutation in position 254, and a threonine (T) to glutamicacid (E) mutation in position 256, numbered according to the EU index asin Kabat (Kabat, et al. (1991) Sequences of Proteins of ImmunologicalInterest, U.S. Public Health Service, National Institutes of Health,Washington, D.C.), introduced into the constant domain of an IgG1. SeeU.S. Pat. No. 7,658,921, which is incorporated by reference herein. Thistype of mutant IgG, referred to as a “YTE mutant” has been shown displayapproximately four-times increased half-life as compared to wild-typeversions of the same antibody (Dall'Acqua et al., J. Biol. Chem.281:23514-24 (2006)). In some aspects, an anti-CD73 antibody orantigen-binding fragment thereof comprising an IgG constant domaincomprises one or more amino acid substitutions of amino acid residues atpositions 251-257, 285-290, 308-314, 385-389, and 428-436, numberedaccording to the EU index as in Kabat, wherein such mutations increasethe serum half-life of the anti-CD73 antibody or antigen-bindingfragment thereof.

In some aspects, a YTE mutant further comprises a substitution atposition 434 of the IgG constant domain, numbered according to the EUindex as in Kabat, with an amino acid selected from the group consistingof tryptophan (W), methionine (M), tyrosine (Y), and serine (S). Inother aspects, a YTE mutant further comprises a substitution at position434 of the IgG constant domain, numbered according to the EU index as inKabat, with an amino acid selected from the group consisting oftryptophan (W), methionine (M), tyrosine (Y), and serine (S), andsubstitution at position 428 of the IgG constant domain, numberedaccording to the EU index as in Kabat, with an amino acid selected fromthe group consisting of threonine (T), leucine (L), phenylalanine (F),and serine (S).

In yet other aspect, a YTE mutant further comprises a substitution atposition 434 of the IgG constant domain, numbered according to the EUindex as in Kabat, with tyrosine (Y), and a substitution at position 257of the IgG constant domain, numbered according to the EU index as inKabat, with leucine (L). In some aspects, a YTE mutant further comprisesa substitution at position 434 of the IgG constant domain, numberedaccording to the EU index as in Kabat, with serine (S), and asubstitution at position 428 of the IgG constant domain, numberedaccording to the EU index as in Kabat, with leucine (L).

In a specific aspect, the anti-CD73 antibody (for example, MEDI9447, aclone 10.3 antibody or a clone 2C5 antibody) or antigen-binding fragmentthereof disclosed herein comprises an IgG1 constant domain comprising amethionine (M) to tyrosine (Y) mutation in position 252, a serine (S) tothreonine (T) mutation in position 254, and a threonine (T) to glutamicacid (E) mutation in position 256 of the IgG1 constant domain, numberedaccording to the EU index as in Kabat.

In certain aspects, the anti-CD73 antibody (for example, MEDI9447, aclone 10.3 antibody or a clone 2C5 antibody) or antigen-binding fragmentthereof disclosed herein comprises at least one IgG constant domainamino acid substitution selected from the group consisting of:

(a) substitution of the amino acid at position 252 with tyrosine (Y),phenylalanine (F), tryptophan (W), or threonine (T);(b) substitution of the amino acid at position 254 with threonine (T);(c) substitution of the amino acid at position 256 with serine (S),arginine (R), glutamine (Q), glutamic acid (E), aspartic acid (D), orthreonine (T);(d) substitution of the amino acid at position 257 with leucine (L);(e) substitution of the amino acid at position 309 with proline (P);(f) substitution of the amino acid at position 311 with serine (S);(g) substitution of the amino acid at position 428 with threonine (T),leucine (L), phenylalanine (F), or serine (S);(h) substitution of the amino acid at position 433 with arginine (R),serine (S), isoleucine (I), proline (P), or glutamine (Q);(i) substitution of the amino acid at position 434 with tryptophan (W),methionine (M), serine (S), histidine (H), phenylalanine (F), ortyrosine; and,(j) a combination of two or more of said substitutions,wherein the positions are numbered according to the EU index as inKabat, and wherein the modified IgG has an increased serum half-lifecompared to the serum half-life of an IgG having the wild-type IgGconstant domain.

In some aspects, the VH and/or VL amino acid sequence of an anti-CD73antibody (for example, MEDI9447, a clone 10.3 antibody or a clone 2C5antibody) or antigen-binding fragment thereof disclosed herein can be85%, 90%, 95%, 96%, 97%, 98% or 99% similar to the VH and VL sequencesset forth above, and comprise 1, 2, 3, 4, 5 or more conservativesubstitutions. A CD73 antibody having VH and VL regions having high(i.e., 80% or greater) sequence similarity or sequence identity to theVH regions of SEQ ID NOs: 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81,82, 83, 84, 85, 87, 111, 113, 114, 115, 116, or 117, and/or VL regionsof SEQ ID NOs: 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70,86, 88, 112, 118, 119, 120, or 121 respectively, can be obtained bymutagenesis (e.g., site-directed or PCR-mediated mutagenesis) of nucleicacid molecules encoding SEQ ID NOs: 57, 58, 59, 60, 61, 62, 63, 64, 65,66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83,84, 85, 86, 87, 88, 111, 112, 113, 114, 115, 116, 117, 118, 119, 120, or121, followed by testing of the encoded altered antibody for retainedfunction using the functional assays described herein.

In some aspects, the Fc domain of an anti-CD73 antibody disclosed hereinor the Fc domain of a fusion protein comprising a CD73-binding fragmentof an antibody disclosed herein has reduced binding to an Fc receptor toreduce cytotoxicity, e.g., via ADCC. In some aspects, the Fc domain ofthe antibody or Fc fusion protein has increased binding to an Fcreceptor to increase cytotoxicity, e.g., via ADCC. In some aspects, theFc domain of the antibody or Fc fusion protein comprises a non-naturallyoccurring ADCC reducing amino acid residue at one or more positionsselected from the group consisting of 234, 235, 236, 237, 238, 239, 240,241, 243, 244, 245, 247, 251, 252, 254, 255, 256, 262, 263, 264, 265,266, 267, 269, 279, 280, 284, 292, 296, 297, 298, 299, 305, 313, 316,325, 326, 327, 328, 329, 330, 331, 332, 333, 334, 339, 341, 343, 370,373, 378, 392, 416, 419, 421, 440, and 443 as numbered by the EU indexas set forth in Kabat. Numerous specific mutations capable of reducingthe ADCC activity of an antibody are known in the art and include, forexample 234F, 235E, 235F, 235Q (or 235Y), 239A, 332Q, 331S andcombinations thereof. For example, see the mutations described inInternational Publication Nos. WO8807089, WO9958572, WO9951642,WO2012175751, WO2011149999, WO2011066501, WO2000042072, WO2011120134,which are herein incorporated by reference in their entireties.Antibodies with reduced ADCC effector function also include those withsubstitution of one or more of Fc region residues 238, 265, 269, 270,297, 327, and 329 (see, e.g., U.S. Pat. No. 6,737,056). Such Fc mutantsalso include Fc mutants with substitutions at two or more of amino acidpositions 265, 269, 270, 297 and 327, including Fc mutant withsubstitution of residues 265 and 297 to alanine (see, e.g., U.S. Pat.No. 7,332,581). Optionally, mutations which reduce both ADCC and CDC canbe incorporated. In some aspects, anti-CD73 antibodies disclosed hereinor antigen-binding fragment thereof comprising mutations that reduce orabolish ADCC and/or CDC can be used to generate antibody drug conjugates(ADC).

In one aspect, the present disclosure provides an anti-CD73 antibody,wherein the antibody is an IgG1, IgG2 or IgG3 and comprises at least onemodification at one or more positions selected from the group consistingof 234, 235, and 331 as numbered by the EU index as set forth in Kabat.In still another specific aspect, the Fc region is an IgG1, IgG2 or IgG3Fc region and the non-naturally occurring amino acids are selected fromthe group consisting of 234F, 235E, 235F, 235Q (or 235Y), 239A, 332Q,331S, 332Q as numbered by the EU index as set forth in Kabat.

In another aspect, the present disclosure provides an anti-CD73antibody, wherein the antibody is an IgG4 and comprises at least onemodification at one or more positions selected from the group consistingof 228 and 235 as numbered by the EU index as set forth in Kabat. Instill another specific aspect, the Fc region is an IgG4 Fc region andthe non-naturally occurring amino acids are selected from the groupconsisting of 228P, 235E and 235Y as numbered by the EU index as setforth in Kabat. In specific aspects, the present disclosure provides ananti-CD73 antibody, wherein the antibody is an IgG1, IgG2, or IgG3 andcomprises modifications at positions (i) 234F, 235E, and 331S; (ii)234F, 235F, and 331S; (iii) 234F, 235Q, and 322Q. In another specificaspect, the present disclosure provides an anti-CD73 antibody, whereinthe antibody is an IgG4 and comprises modifications 228P and 235E.

III. EPITOPE-COMPETING CD73-BINDING MOLECULES

In another aspect, the present disclosure provides CD73-bindingmolecules that bind to the same epitope as do the various anti-CD73antibodies described herein, for example, molecules that bind to thesame epitope as MEDI9447, a clone 10.3 antibody or to the same epitopeas a clone 2C5 antibody.

Such antibodies can be identified based on their ability tocross-compete (e.g., to competitively inhibit the binding of, in astatistically significant manner) with the anti-CD73 antibodiesdisclosed herein, such as the CD730010 antibody, CD730002 antibody,CD730004 antibody, and antigen-binding fragments thereof, in standardCD73 binding assays (e.g., flow cytometry assays, surface plasmonresonance, or solution assays).

Accordingly, in one aspect, the present disclosure provides anti-CD73antibodies and antigen-binding fragments thereof, e.g., human monoclonalantibodies, that compete for binding to CD73 with another anti-CD73antibody or antigen-binding fragment thereof, such as the CD730010antibody, CD730002 antibody, CD730004 antibody, variants thereof (e.g.,MEDI9447, a clone 10.3 antibody or a clone 2C5 antibody), orantigen-binding fragments thereof. The ability of a test antibody toinhibit the binding of, e.g., the CD730010 antibody (or a clone 10.3antibody or an antigen-binding fragment thereof), or the CD730002antibody (or clone 2C5 antibody or an antigen-binding fragment thereof)demonstrates that the test antibody can compete with that antibody forbinding to CD73; such antibody can, according to non-limiting theory,bind to the same or a related (e.g., a structurally similar or spatiallyproximal) epitope on CD73 as the anti-CD73 antibody or antigen-bindingfragment thereof with which it competes. In one aspect, the anti-CD73antibody or antigen-binding fragment thereof that binds to the sameepitope on CD73 as, e.g., the CD730010 antibody (or a clone 10.3antibody or an antigen-binding fragment thereof), or the CD730002antibody (or clone 2C5 antibody or an antigen-binding fragment thereof),is a human monoclonal antibody.

IV. FUNCTIONAL CHARACTERISTICS OF ANTI-CD73 ANTIBODIES

The affinity or avidity of an antibody for an antigen can be determinedexperimentally using any suitable method well known in the art, e.g.,flow cytometry, enzyme-linked immunosorbent assay (ELISA), orradioimmunoassay (RIA), or kinetics (e.g., BIACORE™ analysis). Directbinding assays as well as competitive binding assay formats can bereadily employed. (See, for example, Berzofsky et al., “Antibody-AntigenInteractions,” In Fundamental Immunology, Paul, W. E., Ed., Raven Press:New York, N.Y. (1984); Kuby, Immunology, W. H. Freeman and Company: NewYork, N.Y. (1992); and methods described herein. The measured affinityof a particular antibody-antigen interaction can vary if measured underdifferent conditions (e.g., salt concentration, pH, temperature). Thus,measurements of affinity and other antigen-binding parameters (e.g.,K_(D) or Kd, K_(on), K_(off)) are made with standardized solutions ofantibody and antigen, and a standardized buffer, as known in the art andsuch as the buffer described herein.

It also known in the art that affinities measured using surface plasmonresonance analysis (e.g., BIACORE™) can vary depending on which one ofthe reactants is bound to the chip. In this respect, affinity can bemeasured using a format in which the targeting antibody (e.g., a clone10.3 antibody or a clone 2C5 antibody) is immobilized onto the chip(referred to as an “IgG down” format) or using a format in which thetarget protein (e.g., CD73) is immobilized onto the chip (referred toas, e.g., a “CD73 down” format).

In one aspect of the present disclosure, the anti-CD73 antibody (forexample, MEDI9447, a clone 10.3 antibody or a clone 2C5 antibody) or anantigen-binding fragment thereof specifically binds CD73 and/orantigenic fragments thereof with a dissociation constant or k_(d)(k_(off)/k_(on)) of less than 10⁻⁶ M, or of less than 10⁻⁷ M, or of lessthan 10⁻⁸ M, or of less than 10⁻⁹ M, or of less than 10⁻¹⁰ M, or of lessthan 10⁻¹¹ M, or of less than 10⁻¹² M, or of less than 10⁻¹³ M.

In another aspect, the anti-CD73 antibody (for example, MEDI9447, aclone 10.3 antibody or a clone 2C5 antibody) or an antigen-bindingfragment thereof binds to CD73 and/or antigenic fragments thereof with aK_(off) of less than 1×10⁻³ s⁻¹, or less than 2×10⁻³ s⁻¹. In otheraspects, an anti-CD73 antibody or an antigen-binding fragment thereofbinds to CD73 and antigenic fragments thereof with a K_(off) of lessthan 10⁻³ s⁻¹, less than 5×10⁻³ s⁻¹, less than 10⁻⁴ s⁻¹, less than5×10⁻⁴ s⁻¹, less than 10⁻⁵ s⁻¹, less than 5×10⁻⁵ s⁻¹, less than 10⁻⁶s⁻¹, less than 5×10⁻⁶ s⁻¹, less than less than 5×10⁻⁷ s⁻¹, less than10⁻⁸ s⁻¹, less than 5×10⁻⁸ s⁻¹, less than 10⁻⁹ s⁻¹, less than 5×10⁻⁹s⁻¹, or less than 10⁻¹° s⁻¹.

In another aspect, the anti-CD73 antibody (for example, a clone 10.3antibody or a clone 2C5 antibody) or an antigen-binding fragment thereofbinds to CD73 and/or antigenic fragments thereof with an associationrate constant or k_(on) rate of at least 10⁵ M⁻¹ s⁻¹, at least 5×10⁵ M⁻¹s⁻¹, at least 10⁶ M⁻¹ s⁻¹, at least 5×10⁶ M⁻¹ s⁻¹, at least 10⁷ M⁻¹ s⁻¹,at least 5×10⁷ M⁻¹ s⁻¹, or at least 10⁸ M⁻¹ s⁻¹, or at least 10⁹ M⁻¹s⁻¹.

In some aspects, the anti-CD73 antibody (for example, a clone 10.3antibody or a clone 2C5 antibody) or an antigen-binding fragment thereofbinds to CD73 on the surface of MB-MDA-231 cells with a K_(D) of atleast about 60 pM, at least about 70 pM, at least about 80 pM, at leastabout 90 pM, at least about 100 pM, at least about 110 pM, at leastabout 120 pM, at least about 130 pM, at least about 140 pM, at leastabout 150 pM, at least about 160 pM, or at least about 170 pm, asmeasured by flow cytometry. In one specific aspect, the anti-CD73antibody is a clone 10.3 antibody and it binds to CD73 on the surface ofMB-MDA-231 cells with a K_(D) of about 150 pM as measured by flowcytometry. In another specific aspect, the anti-CD73 antibody is a clone2C5 antibody and it binds to CD73 on the surface of MB-MDA-231 cellswith a K_(D) of about 80 pM as measured by flow cytometry.

In some aspects, the anti-CD73 antibody (for example, MEDI9447, a clone10.3 antibody or a clone 2C5 antibody) or an antigen-binding fragmentthereof binds to CD73 binds on the surface of murine 3T1 cells with aK_(D) of a of at least about 40 pM, at least about 50 pM, at least about60 pM, at least about 70 pM, at least about 80 pM, at least about 90 pM,at least about 100 pM, at least about 120 pM, or at least about 130 pM,as measured by flow cytometry. In one specific aspect, the anti-CD73antibody is a clone 10.3 antibody and it binds to CD73 on the surface ofmurine 3T1 cells with a K_(D) of about 110 pM as measured by flowcytometry. In another specific aspect, the anti-CD73 antibody is a clone2C5 antibody and it binds to CD73 on the surface of murine 3T1 cellswith a K_(D) of about 55 pM as measured by flow cytometry.

In some aspects, the anti-CD73 antibody (for example, MEDI9447, a clone10.3 antibody or a clone 2C5 antibody) or an antigen-binding fragmentthereof binds to CD73 on the surface of cynomolgus MK-1 cells with aK_(D) of a of at least about 40 pM, at least about 50 pM, at least about60 pM, at least about 70 pM, at least about 80 pM, at least about 90 pM,or at least about 100 pM, as measured by flow cytometry. In one specificaspect, the anti-CD73 antibody is a clone 10.3 antibody and it binds toCD73 on the surface of cynomolgus MK-1 cells with a K_(D) of about 80 pMas measured by flow cytometry. In another specific aspect, the anti-CD73antibody is a clone 2C5 antibody and it binds to CD73 on the surface ofcynomolgus MK-1 cells with a K_(D) of about 60 pM as measured by flowcytometry.

In some aspects, the anti-CD73 antibody (for example, MEDI9447, a clone10.3 antibody or a clone 2C5 antibody) or an antigen-binding fragmentthereof binds to human CD73 with a K_(D) of a of at least about 3 pM, atleast about 4 pM, at least about 5 pM, at least about 6 pM, at leastabout 7 pM, at least about 8 pM, at least about 9 pM, or at least about10 pM, as measured by surface plasmon resonance (PROTEON®). In onespecific aspect, the anti-CD73 antibody is a clone 10.3 antibody and itbinds to human CD73 with a K_(D) of about 4 pM as measured by surfaceplasmon resonance (PROTEON®). In another specific aspect, the anti-CD73antibody is a clone 2C5 antibody and it binds to human CD73 with a K_(D)of about 9 pM as measured by surface plasmon resonance (PROTEON®).

In some aspects, the anti-CD73 antibody (for example, MEDI9447, a clone10.3 antibody or a clone 2C5 antibody) or an antigen-binding fragmentthereof disclosed herein binds to murine CD73 with a K_(D) of a of atleast about 1 pM, at least about 2 pM, at least about 3 pM, at leastabout 4 pM, at least about 5 pM, at least about 6 pM, at least about 7pM, at least about 8 pM, at least about 9 pM, at least about 10 pM, atleast about 11 pM, at least about 12 pM, at least about 13 pM, at leastabout 14 pM, at least about 15 pM, at least about 16 pM, at least about17 pM, at least about 18 pM, at least about 19 pM, at least about 20 pM,at least about 21 pM, at least about 22 pM, at least about 23 pM, atleast about 24 pM, or at least about 25 pM, as measured by surfaceplasmon resonance (PROTEON®). In one specific aspect, the anti-CD73antibody is a clone 10.3 antibody and it binds to murine CD73 with aK_(D) of about 1 pM as measured by surface plasmon resonance (PROTEON®).In another specific aspect, the anti-CD73 antibody is a clone 2C5antibody and it binds to murine CD73 with a K_(D) of about 22 pM asmeasured by surface plasmon resonance (PROTEON®).

In some aspects, an anti-CD73 antibody (for example, MEDI9447, a clone10.3 antibody or a clone 2C5 antibody) or an antigen-binding fragmentthereof binds to cynomolgus CD73 with a K_(D) of a of at least about 3pM, at least about 4 pM, at least about 5 pM, at least about 6 pM, atleast about 7 pM, at least about 8 pM, at least about 9 pM, or at leastabout 10 pM, as measured by surface plasmon resonance (PROTEON®). In onespecific aspect, the anti-CD73 antibody is a clone 10.3 antibody and itbinds to cynomolgus CD73 with a K_(D) of about 7 pM as measured by SPR(Proteon). In another specific aspect, the anti-CD73 antibody is a clone2C5 antibody and it binds to cynomolgus CD73 with a K_(D) of about 9 pMas measured by surface plasmon resonance (PROTEON®).

In some aspects, the anti-CD73 antibody (for example, MEDI9447, a clone10.3 antibody or a clone 2C5 antibody) or an antigen-binding fragmentthereof binds to human CD73 with a K_(D) of a of at least about 40 pM,at least about 50 pM, at least about 60 pM, at least about 70 pM, atleast about 80 pM, at least about 90 pM, at least about 100 pM, or atleast about 110 pM, as measured by solution binding. In one specificaspect, the anti-CD73 antibody is a clone 10.3 antibody and it binds tohuman CD73 with a K_(D) of about 80 pM as measured by solution binding.In another specific aspect, the anti-CD73 antibody is a clone 2C5antibody and it binds to human CD73 with a K_(D) of about 80 pM asmeasured by solution binding.

In some aspects, the anti-CD73 antibody (for example, a clone 10.3antibody or a clone 2C5 antibody) or an antigen-binding fragment thereofbinds to murine CD73 with a K_(D) of a of at least about 100 pM, atleast about 200 pM, at least about 300 pM, at least about 400 pM, atleast about 500 pM, at least about 600 pM, at least about 700 pM, atleast about 800 pM, at least about 900 pM, at least about 1000 pM, atleast about 1100 pM, at least about 1200 pM, at least about 1300 pM, atleast about 1400 pM, at least about 1500 pM, at least about 1600 pM, atleast about, or at least about 1700 pM, as measured by solution binding.In one specific aspect, the anti-CD73 antibody is a clone 10.3 antibodyand it binds to murine CD73 with a K_(D) of about 130 pM as measured bysolution binding. In another specific aspect, the anti-CD73 antibody isa clone 2C5 antibody and it binds to murine CD73 with a K_(D) of about1500 pM as measured by solution binding.

In some aspects, the anti-CD73 antibody (for example, a clone 10.3antibody or a clone 2C5 antibody) or an antigen-binding fragment thereofbinds to cynomolgus CD73 with a K_(D) of a of at least about 60 pM, atleast about 70 pM, at least about 80 pM, at least about 90 pM, at leastabout 100 pM, at least about 110 pM, or at least about 120 pM, asmeasured by solution binding. In one specific aspect, the anti-CD73antibody is a clone 10.3 antibody and it binds to cynomolgus CD73 with aK_(D) of about 90 pM as measured by solution binding. In anotherspecific aspect, the anti-CD73 antibody is a clone 2C5 antibody and itbinds to cynomolgus CD73 with a K_(D) of about 100 pM as measured bysolution binding. In particular aspect, MEDI9447 binds CD73 with a K_(D)of about 1×10⁻¹², 5×10⁻¹², 10×10⁻¹², 100×10⁻¹², or 150×10⁻¹².

In some aspects, a CD73-binding molecule disclosed herein, e.g., ananti-CD73 antibody (for example, MEDI9447, a clone 10.3 antibody or aclone 2C5 antibody) or an antigen-binding fragment thereof can relieveAMP-mediated suppression of T cell division. In other aspects, aCD73-binding molecule disclosed herein, e.g., an anti-CD73 antibody (forexample, MEDI9447, a clone 10.3 antibody or a clone 2C5 antibody) or anantigen-binding fragment thereof can rescue ATP-induced T_(eff)suppression by T_(reg).

In some aspects, a CD73-binding molecule disclosed herein, e.g., ananti-CD73 antibody or antigen-binding fragment thereof (for example, aclone 10.3 antibody or a clone 2C5 antibody) can significantly inhibitsyngeneic tumor growth. In one aspect, the tumor is a CT26 mousesyngeneic CRC tumor. In some aspects, a CD73-binding molecule, e.g., ananti-CD73 antibody or antigen-binding fragment thereof disclosed herein(for example, a clone 10.3 antibody or a clone 2C5 antibody) cansignificantly inhibit tumor growth, wherein the tumor is unresponsive totherapy with anti-PD1.

In some aspects, a CD73-binding molecule disclosed herein, e.g., ananti-CD73 antibody or antigen-binding fragment thereof (for example, aclone 10.3 antibody or a clone 2C5 antibody) can be internalized afterbinding to cells. In some aspects, the CD73-binding molecule is anantibody drug conjugate (ADC).

V. PREPARATION OF ANTI-CD73 ANTIBODIES AND ANTIGEN-BINDING FRAGMENTS

Monoclonal anti-CD73 antibodies (e.g., MEDI9447, a clone 10.3 antibodyor a clone 2C5 antibody) and antigen-binding fragments thereof can beprepared using hybridoma methods, such as those described by Kohler andMilstein (1975) Nature 256:495. Using the hybridoma method, a mouse,hamster, or other appropriate host animal, is immunized as describedabove to elicit the production by lymphocytes of antibodies that willspecifically bind to an immunizing antigen. Lymphocytes can also beimmunized in vitro. Following immunization, the lymphocytes are isolatedand fused with a suitable myeloma cell line using, for example,polyethylene glycol, to form hybridoma cells that can then be selectedaway from unfused lymphocytes and myeloma cells. Hybridomas that producemonoclonal antibodies directed specifically against a chosen antigen asdetermined by immunoprecipitation, immunoblotting, or by an in vitrobinding assay (e.g. radioimmunoassay (RIA); enzyme-linked immunosorbentassay (ELISA)) can then be propagated either in in vitro culture usingstandard methods (Goding, Monoclonal Antibodies: Principles andPractice, Academic Press, 1986) or in vivo as ascites tumors in ananimal. The monoclonal antibodies can then be purified from the culturemedium or ascites fluid as described for polyclonal antibodies above.

Alternatively anti-CD73 monoclonal antibodies (for example, MEDI9447, aclone 10.3 antibody or a clone 2C5 antibody) and antigen-bindingfragments thereof can also be made using recombinant DNA methods asdescribed, for example, in U.S. Pat. No. 4,816,567. The polynucleotidesencoding a monoclonal antibody are isolated from mature B-cells orhybridoma cell, such as by RT-PCR using oligonucleotide primers thatspecifically amplify the genes encoding the heavy and light chains ofthe antibody, and their sequence is determined using conventionalprocedures. The isolated polynucleotides encoding the heavy and lightchains are then cloned into suitable expression vectors, which whentransfected into host cells such as E. coli cells, simian COS cells,Chinese hamster ovary (CHO) cells, or myeloma cells that do nototherwise produce immunoglobulin protein, monoclonal antibodies aregenerated by the host cells. Also, recombinant anti-CD73 monoclonalantibodies or antigen-binding fragments thereof of the desired speciescan be isolated from phage display libraries expressing CDRs of thedesired species as described (McCafferty et al., 1990, Nature,348:552-554; Clarkson et al., 1991, Nature, 352:624-628; and Marks etal., 1991, J. Mol. Biol., 222:581-597).

The polynucleotide(s) encoding an anti-CD73 antibody (for example, aclone 10.3 antibody or a clone 2C5 antibody) or antigen-binding fragmentthereof can further be modified in a number of different manners usingrecombinant DNA technology to generate alternative antibodies. In someaspects, the constant domains of the light and heavy chains of, forexample, a mouse monoclonal antibody can be substituted (1) for thoseregions of, for example, a human antibody to generate a chimericantibody or (2) for a non-immunoglobulin polypeptide to generate afusion antibody. In some aspects, the constant regions are truncated orremoved to generate the desired antibody fragment of a monoclonalantibody. Site-directed or high-density mutagenesis of the variableregion can be used to optimize specificity, affinity, etc. of amonoclonal antibody.

In certain aspects, the anti-CD73 antibody (for example, a clone 10.3antibody or a clone 2C5 antibody) or antigen-binding fragment thereof isa human antibody or antigen-binding fragment thereof. Human antibodiescan be directly prepared using various techniques known in the art.Immortalized human B lymphocytes immunized in vitro or isolated from animmunized individual that produce an antibody directed against a targetantigen can be generated (See, e.g., Cole et al., Monoclonal Antibodiesand Cancer Therapy, Alan R. Liss, p. 77 (1985); Boemer et al., 1991, J.Immunol., 147 (1):86-95; and U.S. Pat. No. 5,750,373).

Also, the anti-CD73 human antibody (for example, a clone 10.3 antibodyor a clone 2C5 antibody) or antigen-binding fragment thereof can beselected from a phage library, where that phage library expresses humanantibodies, as described, for example, in Vaughan et al., 1996, Nat.Biotech., 14:309-314, Sheets et al., 1998, Proc. Nat'l. Acad. Sci.,95:6157-6162, Hoogenboom and Winter, 1991, J. Mol. Biol., 227:381, andMarks et al., 1991, J. Mol. Biol., 222:581). Techniques for thegeneration and use of antibody phage libraries are also described inU.S. Pat. Nos. 5,969,108, 6,172,197, 5,885,793, 6,521,404; 6,544,731;6,555,313; 6,582,915; 6,593,081; 6,300,064; 6,653,068; 6,706,484; and7,264,963; and Rothe et al., 2007, J. Mol. Bio.,doi:10.1016/j.jmb.2007.12.018 (each of which is incorporated byreference in its entirety).

Affinity maturation strategies and chain shuffling strategies (Marks etal., 1992, Bio/Technology 10:779-783, incorporated by reference in itsentirety) are known in the art and can be employed to generate highaffinity human antibodies or antigen-binding fragments thereof.

In some aspects, the anti-CD73 monoclonal antibody (for example, a clone10.3 antibody or a clone 2C5 antibody) can be a humanized antibody.Methods for engineering, humanizing or resurfacing non-human or humanantibodies can also be used and are well known in the art. A humanized,resurfaced or similarly engineered antibody can have one or more aminoacid residues from a source that is non-human, e.g., but not limited to,mouse, rat, rabbit, non-human primate or other mammal. These non-humanamino acid residues are replaced by residues that are often referred toas “import” residues, which are typically taken from an “import”variable, constant or other domain of a known human sequence. Suchimported sequences can be used to reduce immunogenicity or reduce,enhance or modify binding, affinity, on-rate, off-rate, avidity,specificity, half-life, or any other suitable characteristic, as knownin the art. In general, the CDR residues are directly and mostsubstantially involved in influencing CD73 binding. Accordingly, part orall of the non-human or human CDR sequences are maintained while thenon-human sequences of the variable and constant regions can be replacedwith human or other amino acids.

Antibodies can also optionally be humanized, resurfaced, engineered orhuman antibodies engineered with retention of high affinity for the CD73antigen and other favorable biological properties. To achieve this goal,humanized (or human) or engineered anti-CD73 antibodies and resurfacedantibodies can be optionally prepared by a process of analysis of theparental sequences and various conceptual humanized and engineeredproducts using three-dimensional models of the parental, engineered, andhumanized sequences. Three-dimensional immunoglobulin models arecommonly available and are familiar to those skilled in the art.Computer programs are available which illustrate and display probablethree-dimensional conformational structures of selected candidateimmunoglobulin sequences. Inspection of these displays permits analysisof the likely role of the residues in the functioning of the candidateimmunoglobulin sequence, i.e., the analysis of residues that influencethe ability of the candidate immunoglobulin to bind its antigen, such asCD73. In this way, framework (FW) residues can be selected and combinedfrom the consensus and import sequences so that the desired antibodycharacteristic, such as increased affinity for the target antigen(s), isachieved.

Humanization, resurfacing or engineering of anti-CD73 antibodies (forexample, a clone 10.3 antibody or a clone 2C5 antibody) orantigen-binding fragments thereof can be performed using any knownmethod, such as but not limited to those described in, Jones et al.,Nature 321:522 (1986); Riechmann et al., Nature 332:323 (1988);Verhoeyen et al., Science 239:1534 (1988)), Sims et al., J. Immunol.151: 2296 (1993); Chothia and Lesk, J. Mol. Biol. 196:901 (1987), Carteret al., Proc. Natl. Acad. Sci. U.S.A. 89:4285 (1992); Presta et al., J.Immunol. 151:2623 (1993), U.S. Pat. Nos. 5,639,641, 5,723,323;5,976,862; 5,824,514; 5,817,483; 5,814,476; 5,763,192; 5,723,323;5,766,886; 5,714,352; 6,204,023; 6,180,370; 5,693,762; 5,530,101;5,585,089; 5,225,539; 4,816,567, 7,557,189; 7,538,195; and 7,342,110;International Application Nos. PCT/US98/16280; PCT/US96/18978;PCT/US91/09630; PCT/US91/05939; PCT/US94/01234; PCT/GB89/01334;PCT/GB91/01134; PCT/GB92/01755; International Patent ApplicationPublication Nos. WO90/14443; WO90/14424; WO90/14430; and European PatentPublication No. EP 229246; each of which is entirely incorporated hereinby reference, including the references cited therein.

Anti-CD73 humanized antibodies and antigen-binding fragments thereof canalso be made in transgenic mice containing human immunoglobulin locithat are capable upon immunization of producing the full repertoire ofhuman antibodies in the absence of endogenous immunoglobulin production.This approach is described in U.S. Pat. Nos. 5,545,807; 5,545,806;5,569,825; 5,625,126; 5,633,425; and 5,661,016.

In certain aspects an anti-CD73 antibody fragment (for example, afragment from a clone 10.3 antibody or from a clone 2C5 antibody) isprovided. Various techniques are known for the production of antibodyfragments. Traditionally, these fragments are derived via proteolyticdigestion of intact antibodies (for example Morimoto et al., 1993,Journal of Biochemical and Biophysical Methods 24:107-117; Brennan etal., 1985, Science, 229:81). In certain aspects, anti-CD73 antibodyfragments are produced recombinantly. Fab, Fv, and scFv antibodyfragments can all be expressed in and secreted from E. coli or otherhost cells, thus allowing the production of large amounts of thesefragments. Such anti-CD73 antibody fragments can also be isolated fromthe antibody phage libraries discussed above. The anti-CD73 antibodyfragments can also be linear antibodies as described in U.S. Pat. No.5,641,870. Other techniques for the production of antibody fragments,e.g., chemical synthesis, will be apparent to the skilled practitioner.

According to the present disclosure, techniques can be adapted for theproduction of single-chain antibodies specific to CD73 (see, e.g., U.S.Pat. No. 4,946,778). In addition, methods can be adapted for theconstruction of Fab expression libraries (see, e.g., Huse et al.,Science 246:1275-1281 (1989)) to allow rapid and effectiveidentification of monoclonal Fab fragments with the desired specificityfor CD73, or derivatives, fragments, analogs or homologs thereof.Antibody fragments can be produced by techniques in the art including,but not limited to: (a) a F(ab′)2 fragment produced by pepsin digestionof an antibody molecule; (b) a Fab fragment generated by reducing thedisulfide bridges of an F(ab′)2 fragment, (c) a Fab fragment generatedby the treatment of the antibody molecule with papain and a reducingagent, and (d) Fv fragments.

An anti-CD73 antibody (for example, a clone 10.3 antibody or a clone 2C5antibody) or an antigen-binding fragment thereof disclosed herein can bemodified in order to increase its serum half-life. This can be achieved,for example, by incorporation of a salvage receptor binding epitope intothe antibody or antibody fragment by mutation of the appropriate regionin the antibody or antibody fragment or by incorporating the epitopeinto a peptide tag that is then fused to the antibody or antibodyfragment at either end or in the middle (e.g., by DNA or peptidesynthesis), or by YTE mutation. Other methods to increase the serumhalf-life of an antibody or antigen-binding fragment thereof, e.g.,conjugation to a heterologous molecule such as PEG are known in the art.

Heteroconjugate anti-CD73 antibodies (for example, a clone 10.3 antibodyor a clone 2C5 antibody) and antigen-binding fragments thereof are alsowithin the scope of the present disclosure. Heteroconjugate antibodiesare composed of two covalently joined antibodies. Such antibodies have,for example, been proposed to target immune cells to unwanted cells(see, e.g., U.S. Pat. No. 4,676,980). It is contemplated that theheteroconjugate anti-CD73 antibodies (for example, a clone 10.3 antibodyor a clone 2C5 antibody) and antigen-binding fragments thereof can beprepared in vitro using known methods in synthetic protein chemistry,including those involving crosslinking agents. For example, immunotoxinscan be constructed using a disulfide exchange reaction or by forming athioether bond. Examples of suitable reagents for this purpose includeiminothiolate and methyl-4-mercaptobutyrimidate.

For the purposes of the present disclosure, it should be appreciatedthat modified anti-CD73 antibodies or antigen-binding fragments thereofcan comprise any type of variable region that provides for theassociation of the antibody or polypeptide with CD73. In this regard,the variable region can comprise or be derived from any type of mammalthat can be induced to mount a humoral response and generateimmunoglobulins against the desired tumor associated antigen. As such,the variable region of the modified anti-CD73 antibodies orantigen-binding fragments thereof can be, for example, of human, murine,non-human primate (e.g., cynomolgus monkeys, macaques, etc.) or lupineorigin. In some aspects both the variable and constant regions of themodified anti-CD73 antibodies or antigen-binding fragments thereof arehuman. In other aspects the variable regions of compatible antibodies(usually derived from a non-human source) can be engineered orspecifically tailored to improve the binding properties or reduce theimmunogenicity of the molecule. In this respect, variable regions can behumanized or otherwise altered through the inclusion of imported aminoacid sequences.

In certain aspects, the variable domains in both the heavy and lightchains of an anti-CD73 antibody (for example, a clone 10.3 antibody or aclone 2C5 antibody) or antigen-binding fragment thereof are altered byat least partial replacement of one or more CDRs and, if necessary, bypartial framework region replacement and sequence changing. Although theCDRs can be derived from an antibody of the same class or even subclassas the antibody from which the framework regions are derived, it isenvisaged that the CDRs will be derived from an antibody of differentclass and in certain aspects from an antibody from a different species.It is not necessary to replace all of the CDRs with the complete CDRsfrom the donor variable region to transfer the antigen-binding capacityof one variable domain to another. Rather, it is only necessary totransfer those residues that are necessary to maintain the activity ofthe antigen-binding site. Given the explanations set forth in U.S. Pat.Nos. 5,585,089, 5,693,761 and 5,693,762, it will be well within thecompetence of those skilled in the art, either by carrying out routineexperimentation or by trial and error testing to obtain a functionalantibody with reduced immunogenicity.

Alterations to the variable region notwithstanding, those skilled in theart will appreciate that the modified anti-CD73 antibodies (for example,a modified clone 10.3 antibody or a modified clone 2C5 antibody) orantigen-binding fragments thereof will comprise antibodies (e.g.,full-length antibodies or immunoreactive fragments thereof) in which atleast a fraction of one or more of the constant region domains has beendeleted or otherwise altered so as to provide desired biochemicalcharacteristics such as increased tumor localization or reduced serumhalf-life when compared with an antibody of approximately the sameimmunogenicity comprising a native or unaltered constant region. In someaspects, the constant region of the modified antibodies will comprise ahuman constant region. Modifications to the constant region compatiblewith this the anti-CD73 molecules disclosed herein comprise additions,deletions or substitutions of one or more amino acids in one or moredomains. That is, the modified antibodies disclosed herein can comprisealterations or modifications to one or more of the three heavy chainconstant domains (CH1, CH2 or CH3) and/or to the light chain constantdomain (CL). In some aspects, modified constant regions wherein one ormore domains are partially or entirely deleted are contemplated. In someaspects, the modified antibodies will comprise domain deleted constructsor variants wherein the entire CH2 domain has been removed (ΔCH2constructs). In some aspects, the omitted constant region domain will bereplaced by a short amino acid spacer (e.g., 10 residues) that providessome of the molecular flexibility typically imparted by the absentconstant region.

Besides their configuration, it is known in the art that the constantregion mediates several effector functions. For example, binding of theC1 component of complement to antibodies activates the complementsystem. Activation of complement is important in the opsonisation andlysis of cell pathogens. The activation of complement also stimulatesthe inflammatory response and can also be involved in autoimmunehypersensitivity. Further, antibodies bind to cells via the Fc region,with a Fc receptor site on the antibody Fc region binding to a Fcreceptor (FcR) on a cell. There are a number of Fc receptors which arespecific for different classes of antibody, including IgG (gammareceptors), IgE (eta receptors), IgA (alpha receptors) and IgM (mureceptors). Binding of antibody to Fc receptors on cell surfacestriggers a number of important and diverse biological responsesincluding engulfment and destruction of antibody-coated particles,clearance of immune complexes, lysis of antibody-coated target cells bykiller cells (called antibody-dependent cell-mediated cytotoxicity, orADCC), release of inflammatory mediators, placental transfer and controlof immunoglobulin production.

In certain aspects, the anti-CD73 antibody (for example, a clone 10.3antibody or a clone 2C5 antibody) or an antigen-binding fragment thereofprovides for altered effector functions that, in turn, affect thebiological profile of the administered antibody or antigen-bindingfragment thereof. For example, the deletion or inactivation (throughpoint mutations or other means) of a constant region domain can reduceFc receptor binding of the circulating modified antibody therebyincreasing tumor localization. In other cases it can be that constantregion modifications, consistent with this disclosure, moderatecomplement binding and thus reduce the serum half-life and nonspecificassociation of a conjugated cytotoxin. Yet other modifications of theconstant region can be used to eliminate disulfide linkages oroligosaccharide moieties that allow for enhanced localization due toincreased antigen specificity or antibody flexibility. Similarly,modifications to the constant region in accordance with this disclosurecan easily be made using well known biochemical or molecular engineeringtechniques well within the purview of the skilled artisan.

In certain aspects, a CD73-binding molecule disclosed herein that is anantibody (for example, a clone 10.3 antibody or a clone 2C5 antibody) orantigen-binding fragment thereof does not have one or more effectorfunctions. For instance, in some aspects, the antibody orantigen-binding fragment thereof has no antibody-dependent cellularcytotoxicity (ADCC) activity and/or no complement-dependent cytotoxicity(CDC) activity. In certain aspects, the anti-CD73 antibody orantigen-binding fragment thereof does not bind to an Fc receptor and/orcomplement factors. In certain aspects, the antibody or antigen-bindingfragment thereof has no effector function.

It will be noted that in certain aspects, the anti-CD73 modifiedantibodies or antigen-binding fragments thereof can be engineered tofuse the CH3 domain directly to the hinge region of the respectivemodified antibodies or fragments thereof. In other constructs it can bedesirable to provide a peptide spacer between the hinge region and themodified CH2 and/or CH3 domains. For example, compatible constructscould be expressed wherein the CH2 domain has been deleted and theremaining CH3 domain (modified or unmodified) is joined to the hingeregion with a 5-20 amino acid spacer. Such a spacer can be added, forinstance, to ensure that the regulatory elements of the constant domainremain free and accessible or that the hinge region remains flexible.However, it should be noted that amino acid spacers can, in some cases,prove to be immunogenic and elicit an unwanted immune response againstthe construct. Accordingly, in certain aspects, any spacer added to theconstruct will be relatively non-immunogenic, or even omittedaltogether, so as to maintain the desired biochemical qualities of themodified antibodies.

Besides the deletion of whole constant region domains, it will beappreciated that the anti-CD73 antibodies and antigen-binding fragmentsthereof of the present disclosure can be provided by the partialdeletion or substitution of a few or even a single amino acid. Forexample, the mutation of a single amino acid in selected areas of theCH2 domain can be enough to substantially reduce Fc binding and therebyincrease tumor localization. Similarly, it can be desirable to simplydelete that part of one or more constant region domains that control theeffector function (e.g., complement C1Q binding) to be modulated. Suchpartial deletions of the constant regions can improve selectedcharacteristics of the antibody or antigen-binding fragment thereof(e.g., serum half-life) while leaving other desirable functionsassociated with the subject constant region domain intact. Moreover, asalluded to above, the constant regions of the disclosed anti-CD73antibodies and antigen-binding fragments thereof can be modified throughthe mutation or substitution of one or more amino acids that enhancesthe profile of the resulting construct. In this respect it is possibleto disrupt the activity provided by a conserved binding site (e.g., Fcbinding) while substantially maintaining the configuration andimmunogenic profile of the modified antibody or antigen-binding fragmentthereof. Certain aspects can comprise the addition of one or more aminoacids to the constant region to enhance desirable characteristics suchas decreasing or increasing effector function or provide for morecytotoxin or carbohydrate attachment. In such aspects it can bedesirable to insert or replicate specific sequences derived fromselected constant region domains.

The present disclosure also provides variants and equivalents which aresubstantially homologous to the chimeric, humanized and human anti-CD73antibodies, or antigen-binding fragments thereof, set forth herein.These can contain, for example, conservative substitution mutations,i.e., the substitution of one or more amino acids by similar aminoacids. For example, conservative substitution refers to the substitutionof an amino acid with another within the same general class such as, forexample, one acidic amino acid with another acidic amino acid, one basicamino acid with another basic amino acid or one neutral amino acid byanother neutral amino acid. What is intended by a conservative aminoacid substitution is well known in the art.

An anti-CD73 antibody or antigen-binding fragment thereof can be furthermodified to contain additional chemical moieties not normally part ofthe protein. Those derivatized moieties can improve the solubility, thebiological half-life or absorption of the protein. The moieties can alsoreduce or eliminate any desirable side effects of the proteins and thelike. An overview for those moieties can be found in Remington'sPharmaceutical Sciences, 20th ed., Mack Publishing Co., Easton, Pa.(2000).

VI. POLYNUCLEOTIDES ENCODING CD73-BINDING MOLECULES

In certain aspects, the present disclosure encompasses polynucleotidescomprising nucleic acid sequences that encode a polypeptide thatspecifically binds CD73 or an antigen-binding fragment thereof. Forexample, the present disclosure provides a polynucleotide comprising anucleic acid sequence that encodes an anti-CD73 antibody (e.g., a clone10.3 antibody or a clone 2C5 antibody) or encodes an antigen-bindingfragment of such an antibody. The polynucleotides of the presentdisclosure can be in the form of RNA or in the form of DNA. DNA includescDNA, genomic DNA, and synthetic DNA; and can be double-stranded orsingle-stranded, and if single stranded can be the coding strand ornon-coding (anti-sense) strand.

In certain aspects, the polynucleotides are isolated. In certainaspects, the polynucleotides are substantially pure. In certain aspectsthe polynucleotides comprise the coding sequence for the maturepolypeptide fused in the same reading frame to a polynucleotide whichaids, for example, in expression and secretion of a polypeptide from ahost cell (e.g., a leader sequence which functions as a secretorysequence for controlling transport of a polypeptide from the cell). Thepolypeptide having a leader sequence is a preprotein and can have theleader sequence cleaved by the host cell to form the mature form of thepolypeptide. The polynucleotides can also encode for a CD73-bindingproprotein which is the mature protein plus additional 5′ amino acidresidues.

In certain aspects the polynucleotides comprise the coding sequence forthe mature CD73-binding polypeptide, e.g., an anti-CD73 antibody (e.g.,a clone 10.3 antibody or a clone 2C5 antibody) or an antigen-bindingfragment thereof fused in the same reading frame to a marker sequencethat allows, for example, for purification of the encoded polypeptide.For example, the marker sequence can be a hexa-histidine tag (SEQ ID NO:146) supplied by a pQE-9 vector to provide for purification of themature polypeptide fused to the marker in the case of a bacterial host,or the marker sequence can be a hemagglutinin (HA) tag derived from theinfluenza hemagglutinin protein when a mammalian host (e.g., COS-7cells) is used.

The present disclosure also provides variants of the describedpolynucleotides encoding, for example, CD73-binding fragments, analogs,and derivatives of the CD73-binding molecules disclosed herein (e.g., aclone 10.3 antibody or a clone 2C5 antibody).

The polynucleotide variants can contain alterations in the codingregions, non-coding regions, or both. In some aspects the polynucleotidevariants contain alterations which produce silent substitutions,additions, or deletions, but do not alter the properties or activitiesof the encoded polypeptide. In some aspects, nucleotide variants areproduced by silent substitutions due to the degeneracy of the geneticcode. Polynucleotide variants can be produced for a variety of reasons,e.g., to optimize codon expression for a particular host (change codonsin the human mRNA to those preferred by a bacterial host such as E.coli). Vectors and cells comprising the polynucleotides described hereinare also provided.

In some aspects a DNA sequence encoding a CD73-binding molecule, e.g.,an anti-CD73 antibody (e.g., a clone 10.3 antibody or a clone 2C5antibody) or an antigen-binding fragment thereof can be constructed bychemical synthesis using an oligonucleotide synthesizer. Sucholigonucleotides can be designed based on the amino acid sequence of thedesired polypeptide and selecting those codons that are favored in thehost cell in which the recombinant polypeptide of interest will beproduced. Standard methods can be applied to synthesize an isolatedpolynucleotide sequence encoding an isolated polypeptide of interest.For example, a complete amino acid sequence can be used to construct aback-translated gene. Further, a DNA oligomer containing a nucleotidesequence coding for the particular isolated polypeptide can besynthesized. For example, several small oligonucleotides coding forportions of the desired polypeptide can be synthesized and then ligated.The individual oligonucleotides typically contain 5′ or 3′ overhangs forcomplementary assembly.

Once assembled (by synthesis, site-directed mutagenesis or anothermethod), the polynucleotide sequences encoding a particular isolatedpolypeptide of interest will be inserted into an expression vector andoperatively linked to an expression control sequence appropriate forexpression of the protein in a desired host. Proper assembly can beconfirmed by nucleotide sequencing, restriction mapping, and expressionof a biologically active polypeptide in a suitable host. As is wellknown in the art, in order to obtain high expression levels of atransfected gene in a host, the gene must be operatively linked totranscriptional and translational expression control sequences that arefunctional in the chosen expression host.

In certain aspects, recombinant expression vectors are used to amplifyand express DNA encoding anti-CD73 antibodies (e.g., a clone 10.3antibody or a clone 2C5 antibody) or antigen-binding fragments thereof.Recombinant expression vectors are replicable DNA constructs which havesynthetic or cDNA-derived DNA fragments encoding a polypeptide chain ofan anti-CD73 antibody or and antigen-binding fragment thereof,operatively linked to suitable transcriptional or translationalregulatory elements derived from mammalian, microbial, viral or insectgenes.

A transcriptional unit generally comprises an assembly of (1) a geneticelement or elements having a regulatory role in gene expression, forexample, transcriptional promoters or enhancers, (2) a structural orcoding sequence which is transcribed into mRNA and translated intoprotein, and (3) appropriate transcription and translation initiationand termination sequences, as described in detail below. Such regulatoryelements can include an operator sequence to control transcription. Theability to replicate in a host, usually conferred by an origin ofreplication, and a selection gene to facilitate recognition oftransformants can additionally be incorporated. DNA regions areoperatively linked when they are functionally related to each other. Forexample, DNA for a signal peptide (secretory leader) is operativelylinked to DNA for a polypeptide if it is expressed as a precursor whichparticipates in the secretion of the polypeptide; a promoter isoperatively linked to a coding sequence if it controls the transcriptionof the sequence; or a ribosome binding site is operatively linked to acoding sequence if it is positioned so as to permit translation.Structural elements intended for use in yeast expression systems includea leader sequence enabling extracellular secretion of translated proteinby a host cell. Alternatively, where recombinant protein is expressedwithout a leader or transport sequence, it can include an N-terminalmethionine residue. This residue can optionally be subsequently cleavedfrom the expressed recombinant protein to provide a final product.

The choice of expression control sequence and expression vector willdepend upon the choice of host. A wide variety of expression host/vectorcombinations can be employed. Useful expression vectors for eukaryotichosts, include, for example, vectors comprising expression controlsequences from SV40, bovine papilloma virus, adenovirus andcytomegalovirus. Useful expression vectors for bacterial hosts includeknown bacterial plasmids, such as plasmids from E. coli, including pCR1, pBR322, pMB9 and their derivatives, wider host range plasmids, suchas M13 and filamentous single-stranded DNA phages.

Suitable host cells for expression of a CD73-binding molecule, e.g., ananti-CD73 antibody (e.g., a clone 10.3 antibody or a clone 2C5 antibody)or antigen-binding fragment thereof include prokaryotes, yeast, insector higher eukaryotic cells under the control of appropriate promoters.Prokaryotes include gram negative or gram positive organisms, forexample E. coli or bacilli. Higher eukaryotic cells include establishedcell lines of mammalian origin as described below. Cell-free translationsystems could also be employed. Appropriate cloning and expressionvectors for use with bacterial, fungal, yeast, and mammalian cellularhosts are described by Pouwels et al. (Cloning Vectors: A LaboratoryManual, Elsevier, N. Y., 1985), the relevant disclosure of which ishereby incorporated by reference. Additional information regardingmethods of protein production, including antibody production, can befound, e.g., in U.S. Patent Publication No. 2008/0187954, U.S. Pat. Nos.6,413,746 and 6,660,501, and International Patent Publication No. WO04009823, each of which is hereby incorporated by reference herein inits entirety.

Various mammalian or insect cell culture systems can also beadvantageously employed to express recombinant CD73-binding molecules,e.g., anti-CD73 antibodies (e.g., a clone 10.3 antibody or a clone 2C5antibody) or antigen-binding fragments thereof. Expression ofrecombinant proteins in mammalian cells can be performed because suchproteins are generally correctly folded, appropriately modified andcompletely functional.

Examples of suitable mammalian host cell lines include HEK-293 andHEK-293T, the COS-7 lines of monkey kidney cells, described by Gluzman(Cell 23:175, 1981), and other cell lines including, for example, Lcells, C127, 3T3, Chinese hamster ovary (CHO), NSO, HeLa and BHK celllines. Mammalian expression vectors can comprise nontranscribed elementssuch as an origin of replication, a suitable promoter and enhancerlinked to the gene to be expressed, and other 5′ or 3′ flankingnontranscribed sequences, and 5′ or 3′ nontranslated sequences, such asnecessary ribosome binding sites, a polyadenylation site, splice donorand acceptor sites, and transcriptional termination sequences.Baculovirus systems for production of heterologous proteins in insectcells are reviewed by Luckow and Summers, BioTechnology 6:47 (1988).

CD73-binding molecules, e.g., anti-CD73 antibodies (e.g., a clone 10.3antibody or a clone 2C5 antibody) or antigen-binding fragments thereofproduced by a transformed host can be purified according to any suitablemethod. Such standard methods include chromatography (e.g., ionexchange, affinity and sizing column chromatography), centrifugation,differential solubility, or by any other standard technique for proteinpurification. Affinity tags such as hexahistidine (SEQ ID NO: 146),maltose binding domain, influenza coat sequence andglutathione-S-transferase can be attached to the protein to allow easypurification by passage over an appropriate affinity column. Isolatedproteins can also be physically characterized using such techniques asproteolysis, nuclear magnetic resonance and x-ray crystallography.

For example, supernatants from systems which secrete recombinant proteininto culture media can be first concentrated using a commerciallyavailable protein concentration filter, for example, an AMICON® orMillipore PELLICON® ultrafiltration unit. Following the concentrationstep, the concentrate can be applied to a suitable purification matrix.Alternatively, an anion exchange resin can be employed, for example, amatrix or substrate having pendant diethylaminoethyl (DEAE) groups. Thematrices can be acrylamide, agarose, dextran, cellulose or other typescommonly employed in protein purification. Alternatively, a cationexchange step can be employed. Suitable cation exchangers includevarious insoluble matrices comprising sulfopropyl or carboxymethylgroups. Finally, one or more reversed-phase high performance liquidchromatography (RP-HPLC) steps employing hydrophobic RP-HPLC media,e.g., silica gel having pendant methyl or other aliphatic groups, can beemployed to further purify a CD73-binding molecule (e.g., a clone 10.3antibody or a clone 2C5 antibody). Some or all of the foregoingpurification steps, in various combinations, can also be employed toprovide a homogeneous recombinant protein.

A recombinant CD73-binding protein, e.g., an anti-CD73 antibody (e.g., aclone 10.3 antibody or a clone 2C5 antibody) or antigen-binding fragmentthereof produced in bacterial culture can be isolated, for example, byinitial extraction from cell pellets, followed by one or moreconcentration, salting-out, aqueous ion exchange or size exclusionchromatography steps. High performance liquid chromatography (HPLC) canbe employed for final purification steps. Microbial cells employed inexpression of a recombinant protein can be disrupted by any convenientmethod, including freeze-thaw cycling, sonication, mechanicaldisruption, or use of cell lysing agents.

Methods known in the art for purifying antibodies and other proteinsalso include, for example, those described in U.S. Patent PublicationNos. 2008/0312425, 2008/0177048, and 2009/0187005, each of which ishereby incorporated by reference herein in its entirety.

In certain aspects, the CD73-binding molecule is a polypeptide that isnot an antibody. A variety of methods for identifying and producingnon-antibody polypeptides that bind with high affinity to a proteintarget are known in the art. See, e.g., Skerra, Curr. Opin. Biotechnol.,18:295-304 (2007), Hosse et al., Protein Science, 15:14-27 (2006), Gillet al., Curr. Opin. Biotechnol., 17:653-658 (2006), Nygren, FEBS J.,275:2668-76 (2008), and Skerra, FEBS J., 275:2677-83 (2008), each ofwhich is incorporated by reference herein in its entirety. In certainaspects, phage display technology can been used to identify/produce anCD73-binding polypeptide. In certain aspects, the polypeptide comprisesa protein scaffold of a type selected from the group consisting ofprotein A, a lipocalin, a fibronectin domain (e.g., a fibronectin domainsuch as a Tenascin-3 Fn III domain), an ankyrin consensus repeat domain,and thioredoxin.

VI. TREATMENT METHODS USING THERAPEUTIC ANTI-CD73 ANTIBODIES

The present disclosure provides methods directed to the use of anti-CD73binding molecules, e.g., antibodies, including antigen-bindingfragments, variants, and derivatives thereof (for example, a clone 10.3antibody or a clone 2C5 antibody), to treat patients having a diseaseassociated with CD73 expression or CD73-expressing cells, e.g., cancer.In some specific aspects, such cancer is lung cancer, breast cancer,colon cancer, and lymphoma.

By “CD73-expressing cell” is meant a cell expressing CD73. CD73 can bemembrane-bound via glycosyl phosphatidylinositol-anchoring and also bepresent as a soluble protein. Methods for detecting CD73 expression incells and other suitable samples are well known in the art and include,but are not limited to immunohistochemistry, flow cytometry, Westernblot, ELISA, and the like.

Though the following discussion refers to diagnostic methods andtreatment of various diseases and disorders with an CD73-bindingmolecule of the present disclosure (e.g., a clone 10.3 antibody or aclone 2C5 antibody), the methods described herein are also applicable toany other anti-CD73 antibodies, and the antigen-binding fragments,variants, and derivatives (e.g., fusion proteins or conjugates) of theseanti-CD73 antibodies that retain the desired properties of the anti-CD73antibodies disclosed herein, e.g., being capable of specifically bindingCD73 and neutralizing its 5′-nucleotidase activity. In some aspects,CD73-binding molecules are human or humanized antibodies that do notmediate human ADCC, or are anti-CD73 antibodies that are engineered suchthat they do not mediate ADCC.

In some aspects, the CD73-binding molecule is a CD730010 antibody orantigen-binding fragment thereof, a clone 10.3 antibody or anantigen-binding fragment thereof, a CD730002 antibody or antigen-bindingfragment thereof, a clone 2C5 antibody or an antigen-binding fragmentthereof, or a CD73004 antibody or antigen-binding fragment thereof. Inother aspects, the CD73-binding molecule is a clone 10.3 mutantantibody. In some aspects, the CD73-binding molecule is a clone 10.3monoclonal antibody. In some aspects, the CD73-binding molecule is aclone 10.3 monoclonal antibody engineered to extend serum half-life. Inother aspects, the CD73-binding molecule is a clone 10.3 YTE mutantantibody. In other aspects, the CD73-binding molecule is a clone 2C5mutant antibody. In some aspects, the CD73-binding molecule is a clone2C5 monoclonal antibody. In some aspects, the CD73-binding molecule is aclone 2C5 monoclonal antibody engineered to extend serum half-life. Inother aspects, the CD73-binding molecule is a clone 2C5 YTE mutantantibody.

In one aspect, treatment includes the application or administration ofan anti-CD73 binding molecule, e.g., an antibody (e.g., a clone 10.3antibody or a clone 2C5 antibody) or antigen-binding fragment, variant,or derivative thereof of the current disclosure to a subject or patient,or application or administration of the anti-CD73 binding molecule to anisolated tissue or cell line from a subject or patient, where thesubject or patient has a disease, a symptom of a disease, or apredisposition toward a disease. In another aspect, treatment is alsointended to include the application or administration of apharmaceutical composition comprising the anti-CD73 binding molecule,e.g., an antibody or antigen-binding fragment, variant, or derivativethereof of the current disclosure to a subject or patient, orapplication or administration of a pharmaceutical composition comprisingthe anti-CD73 binding molecule to an isolated tissue or cell line from asubject or patient, who has a disease, a symptom of a disease, or apredisposition toward a disease.

The anti-CD73 binding molecules, e.g., antibodies (e.g., a clone 10.3antibody or a clone 2C5 antibody) or antigen-binding fragments,variants, or derivatives thereof of the present disclosure are usefulfor the treatment of various cancers. In one aspect, the presentdisclosure provides anti-CD73 binding molecules, e.g., antibodies (e.g.,a clone 10.3 antibody or a clone 2C5 antibody) or antigen-bindingfragments, variants, or derivatives thereof for use as a medicament, inparticular for use in the treatment or prophylaxis of cancer (e.g.,colon cancer, breast cancer, lymphoma, or non-small cell carcinoma. Insome aspect, the cancer presents a prometastatic phenotype. In someaspects, the cancer is a metastatic cancer. In some aspects, theanti-CD73 binding molecules disclosed herein can trigger adaptiveanti-tumor activity and/or inhibit metastasis. In some particularaspects, the anti-Cd73 binding molecules disclosed herein can inhibitmetastasis in breast cancer.

In accordance with the methods of the present disclosure, at least oneanti-CD73 binding molecule, e.g., an antibody (e.g., a clone 10.3antibody or a clone 2C5 antibody) or antigen-binding fragment, variant,or derivative thereof as defined elsewhere herein is used to promote apositive therapeutic response with respect to cancer. The term “positivetherapeutic response” with respect to cancer treatment refers to animprovement in the disease in association with the activity of theseanti-CD73 binding molecules, e.g., antibodies or antigen-bindingfragments, variants, or derivatives thereof, and/or an improvement inthe symptoms associated with the disease. Thus, for example, animprovement in the disease can be characterized as a complete response.By “complete response” is intended an absence of clinically detectabledisease with normalization of any previously test results.Alternatively, an improvement in the disease can be categorized as beinga partial response. A “positive therapeutic response” encompasses areduction or inhibition of the progression and/or duration of cancer,the reduction or amelioration of the severity of cancer, and/or theamelioration of one or more symptoms thereof resulting from theadministration of an anti-CD73 binding molecule disclosed herein.

In specific aspects, such terms refer to one, two or three or moreresults following the administration of anti-CD73 binding moleculesdisclosed herein: (1) a stabilization, reduction or elimination of thecancer cell population; (2) a stabilization or reduction in cancergrowth; (3) an impairment in the formation of cancer; (4) eradication,removal, or control of primary, regional and/or metastatic cancer; (5) areduction in mortality; (6) an increase in disease-free, relapse-free,progression-free, and/or overall survival, duration, or rate; (7) anincrease in the response rate, the durability of response, or number ofpatients who respond or are in remission; (8) a decrease inhospitalization rate, (9) a decrease in hospitalization lengths, (10)the size of the cancer is maintained and does not increase or increasesby less than 10%, preferably less than 5%, preferably less than 4%,preferably less than 2%, and (12) an increase in the number of patientsin remission.

Clinical response can be assessed using screening techniques such asmagnetic resonance imaging (MRI) scan, x-radiographic imaging, computedtomographic (CT) scan, flow cytometry or fluorescence-activated cellsorter (FACS) analysis, histology, gross pathology, and blood chemistry,including but not limited to changes detectable by ELISA, RIA,chromatography, and the like. In addition to these positive therapeuticresponses, the subject undergoing therapy with the anti-CD73 bindingmolecule, e.g., an antibody or antigen-binding fragment, variant, orderivative thereof, can experience the beneficial effect of animprovement in the symptoms associated with the disease.

The anti-CD73 binding molecules, e.g., antibodies (e.g., a clone 10.3antibody or a clone 2C5 antibody) or antigen-binding fragments,variants, or derivatives thereof disclosed herein can be used incombination with any known therapies for cancer, including any agent orcombination of agents that are known to be useful, or which have beenused or are currently in use, for treatment of cancer, e.g., coloncancer, lung cancer (e.g., non-small cell carcinoma), lymphoma, breastcancerin specific aspects the CD73-binding molecules disclosed herein,e.g., antibodies (e.g., a clone 10.3 antibody or a clone 2C5 antibody)or antigen-binding fragments thereof, can be administered in combinationwith antibodies or antibody fragments targeting, for example, PD-1(programmed death 1 protein), In some aspects, the anti-PD-1 antibody ispembrolizumab (KEYTRUDA®, formerly lambrolizumab, also known as MK-3475)or an antigen-binding fragment thereof. In some aspects, the anti-PD-1antibody is nivolumab (BMS-936558, MDX-1106, ONO-4538, OPDIVA®) or anantigen-binding fragment thereof. In some aspects, the anti-PD-1antibody is MEDI4736 or an antigen-binding fragment thereof.

In some aspects, the CD73-binding molecules disclosed herein (forexample, a clone 10.3 antibody or a clone 2C5 antibody) can beadministered in combination with an anti-PD-1 antibody. In some aspects,the administration of a combination treatment comprising an CD73-bindingmolecule disclosed herein (for example, MEDI9447, a clone 10.3 antibodyor a clone 2C5 antibody) in combination with an anti-PD-1 antibody, canincrease survival by about 10%, about 20%, about 30%, about 40%, about50%, about 60%, about 70%, about 80%, about 90%, or about 100% comparedto untreated subjects or subjects treated with a monotherapy (e.g., ananti-PD-1 antibody without an anti-CD73 antibody). In some aspects, theadministration of a combination treatment comprising an CD73-bindingmolecule disclosed herein (for example, a clone 10.3 antibody or a clone2C5 antibody) in combination with an anti-PD-1 antibody, can increasesurvival by about 2-fold, about 3-fold, about 4-fold, about 5-fold,about 6-fold, about 7-fold, about 8-fold, about 9-fold, or about 10-foldcompared to untreated subjects or subjects treated with a monotherapy(e.g., an anti-PD-1 antibody without an anti-CD73 antibody).

Where the combined therapies comprise administration of an anti-CD73binding molecule in combination with administration of anothertherapeutic agent (e.g., an anti-PD1), the methods disclosed hereinencompass co-administration, using separate formulations or a singlepharmaceutical formulation, and consecutive administration in eitherorder. In some aspects, the anti-CD73 antibodies described herein (forexample, a clone 10.3 antibody or a clone 2C5 antibody) are administeredin combination with other drugs, wherein the antibody or antigen-bindingfragment, variant, or derivative thereof and the therapeutic agent(s)can be administered sequentially, in either order, or simultaneously(i.e., concurrently or within the same time frame).

The combination therapy can provide “synergy” and prove “synergistic”,i.e., the effect achieved when the active ingredients used together isgreater than the sum of the effects that results from using thecompounds separately. A synergistic effect can be attained when theactive ingredients are: (1) co-formulated and administered or deliveredsimultaneously in a combined, unit dosage formulation; (2) delivered byalternation or in parallel as separate formulations; or (3) by someother regimen. When delivered in alternation therapy, a synergisticeffect can be attained when the compounds are administered or deliveredsequentially, e.g., by different injections in separate syringes. Ingeneral, during alternation therapy, an effective dosage of each activeingredient is administered sequentially, i.e., serially, whereas incombination therapy, effective dosages of two or more active ingredientsare administered together.

A further aspect is the use of anti-CD73 binding molecules, e.g.,antibodies or antigen-binding fragments, variants, or derivativesthereof (for example, a clone 10.3 antibody or a clone 2C5 antibody),for diagnostic monitoring of protein levels in tissue as part of aclinical testing procedure, e.g., to determine the efficacy of a giventreatment regimen. For example, detection can be facilitated by couplingthe antibody to a detectable substance.

Examples of detectable substances include various enzymes, prostheticgroups, fluorescent materials, luminescent materials, bioluminescentmaterials, and radioactive materials. Examples of suitable enzymesinclude horseradish peroxidase, alkaline phosphatase, β-galactosidase,or acetylcholinesterase; examples of suitable prosthetic group complexesinclude streptavidin/biotin and avidin/biotin; examples of suitablefluorescent materials include umbelliferone, fluorescein, fluoresceinisothiocyanate, rhodamine, dichlorotriazinylamine fluorescein, dansylchloride or phycoerythrin; an example of a luminescent material includesluminol; examples of bioluminescent materials include luciferase,luciferin, and aequorin; and examples of suitable radioactive materialinclude ¹²⁵I, ¹³¹I, ³⁵S, or ³H.

VII. PHARMACEUTICAL COMPOSITIONS AND METHODS OF ADMINISTRATION

Methods of preparing and administering anti-CD73 binding molecules,e.g., antibodies, or antigen-binding fragments, variants, or derivativesthereof (e.g., a clone 10.3 antibody or a clone 2C5 antibody) to asubject in need thereof are well known to or are readily determined bythose skilled in the art. The route of administration of the anti-CD73binding molecule, e.g., an antibody, or antigen-binding fragment,variant, or derivative thereof can be, for example, oral, parenteral, byinhalation or topical. The term parenteral as used herein includes,e.g., intravenous, intraarterial, intraperitoneal, intramuscular,subcutaneous, rectal, or vaginal administration. However, in othermethods compatible with the teachings herein, anti-CD73 bindingmolecules, e.g., antibodies, or antigen-binding fragments, variants, orderivatives thereof, of the present disclosure can be delivered directlyto the site of the adverse cellular population thereby increasing theexposure of the diseased tissue to the therapeutic agent.

As discussed herein, anti-CD73 binding molecules, e.g., antibodies, orantigen-binding fragments, variants, or derivatives thereof of thepresent disclosure (for example, a clone 10.3 antibody or a clone 2C5antibody) can be administered in a pharmaceutically effective amount forthe in vivo treatment of CD73-expressing cell-mediated diseases such ascertain types of cancers.

The pharmaceutical compositions used in this disclosure can comprisepharmaceutically acceptable carriers, including, e.g., water, ionexchangers, proteins, buffer substances, and salts. Preservatives andother additives can also be present. The carrier can be a solvent ordispersion medium. Suitable formulations for use in therapeutic methodsdisclosed herein are described in Remington's Pharmaceutical Sciences(Mack Publishing Co.) 16th ed. (1980).

In any case, sterile injectable solutions can be prepared byincorporating an active compound (e.g., an anti-CD73 antibody, orantigen-binding fragment, variant, or derivative thereof, for example aclone 10.3 antibody or a clone 2C5 antibody, by itself or in combinationwith other active agents) in the required amount in an appropriatesolvent followed by filtered sterilization. Further, the preparationscan be packaged and sold in the form of a kit. Such articles ofmanufacture can have labels or package inserts indicating that theassociated compositions are useful for treating a subject sufferingfrom, or predisposed to a disease or disorder.

Parenteral formulations can be a single bolus dose, an infusion or aloading bolus dose followed with a maintenance dose. These compositionscan be administered at specific fixed or variable intervals, e.g., oncea day, or on an “as needed” basis.

The composition can be administered as a single dose, multiple doses orover an established period of time in an infusion. Dosage regimens alsocan be adjusted to provide the optimum desired response (e.g., atherapeutic or prophylactic response).

Therapeutically effective doses of the compositions of the presentdisclosure, for treatment of CD73-expressing cell-mediated diseases,such as certain types of cancers including e.g., colon cancer, varydepending upon many different factors, including means ofadministration, target site, physiological state of the patient, whetherthe patient is human or an animal, other medications administered, andwhether treatment is prophylactic or therapeutic. Usually, the patientis a human, but non-human mammals including transgenic mammals can alsobe treated. Treatment dosages can be titrated using routine methodsknown to those of skill in the art to optimize safety and efficacy.

The amount of at least one anti-CD73 binding molecule, e.g., antibody orbinding fragment, variant, or derivative thereof (for example, a clone10.3 antibody or a clone 2C5 antibody) to be administered is readilydetermined by one of ordinary skill in the art without undueexperimentation given the disclosure of the present disclosure. Factorsinfluencing the mode of administration and the respective amount of atleast one anti-CD73 binding molecule, e.g., antibody, antigen-bindingfragment, variant or derivative thereof include, but are not limited to,the severity of the disease, the history of the disease, and the age,height, weight, health, and physical condition of the individualundergoing therapy. Similarly, the amount of anti-CD73 binding molecule,e.g., antibody, or fragment, variant, or derivative thereof, to beadministered will be dependent upon the mode of administration andwhether the subject will undergo a single dose or multiple doses of thisagent.

The present disclosure also provides for the use of an anti-CD73 bindingmolecule, e.g., an antibody or antigen-binding fragment, variant, orderivative thereof (for example, a clone 10.3 antibody or a clone 2C5antibody), in the manufacture of a medicament for treating a type ofcancer, including, e.g., colon cancer.

The disclosure also provides for the use of an anti-CD73 bindingmolecule, e.g., antibody, or antigen-binding fragment, variant, orderivative thereof (for example, a clone 10.3 antibody or a clone 2C5antibody), in the manufacture of a medicament for treating a subject fortreating a type of cancer. In certain aspects, the medicament is used ina subject that has been pretreated with at least one other therapy.

By “pretreated” or “pretreatment” is intended the subject has receivedone or more other therapies (e.g., been treated with at least one otheranti-cancer therapy) prior to receiving the medicament comprising theanti-CD73 binding molecule, e.g., antibody or antigen-binding fragment,variant, or derivative thereof (for example, a clone 10.3 antibody or aclone 2C5 antibody). It is not necessary that the subject was aresponder to pretreatment with the prior therapy or therapies. Thus, thesubject that receives the medicament comprising the anti-CD73 bindingmolecule, e.g., an antibody or antigen-binding fragment, variant, orderivative thereof could have responded, or could have failed to respondto pretreatment with the prior therapy, or to one or more of the priortherapies where pretreatment comprised multiple therapies.

The present disclosure also provides for the co-administration of ananti-CD73 binding molecule, e.g., antibody, or antigen-binding fragment,variant, or derivative thereof (for example, a clone 10.3 antibody or aclone 2C5 antibody) and at least one other therapy. The anti-CD73antibody and the at least one other therapy can be co-administeredtogether in a single composition or can be co-administered together atthe same time or overlapping times in separate compositions. In someaspects, the anti-CD73 antibody can be co-administered with, forexample, an antibody that targets PD-1 (programmed death 1 protein Thepresent disclosure also provides for the use of an anti-CD73 bindingmolecule, e.g., antibody, or antigen-binding fragment, variant, orderivative thereof (for example, a clone 10.3 antibody or a clone 2C5antibody), in the manufacture of a medicament for treating a subject fortreating cancer, wherein the anti-CD73 binding molecule is administeredbefore a subject has been treated with at least one other therapy.

VIII. DIAGNOSTICS

The present disclosure further provides diagnostic methods useful duringdiagnosis of CD73-expressing cell-mediated diseases such as certaintypes of cancer, which involves measuring the expression level of CD73protein in tissue or other cells or body fluid from an individual andcomparing the measured expression level with a standard CD73 expressionlevel in normal tissue or body fluid, whereby an increase in theexpression level compared to the standard is indicative of a disorder.

The anti-CD73 antibodies disclosed herein and antigen-binding fragments,variants, and derivatives thereof (e.g., a clone 10.3 antibody or aclone 2C5 antibody), can be used to assay CD73 protein levels in abiological sample using classical immunohistological methods known tothose of skill in the art (e.g., see Jalkanen, et al., J. Cell. Biol.101:976-985 (1985); Jalkanen et al., J. Cell Biol. 105:3087-3096(1987)). Other antibody-based methods useful for detecting CD73 proteinexpression include immunoassays, such as the enzyme linked immunosorbentassay (ELISA), immunoprecipitation, or Western blotting. Suitable assaysare described in more detail elsewhere herein.

By “assaying the expression level of CD73 polypeptide” is intendedqualitatively or quantitatively measuring or estimating the level ofCD73 polypeptide in a first biological sample either directly (e.g., bydetermining or estimating absolute protein level) or relatively (e.g.,by comparing to the disease associated polypeptide level in a secondbiological sample). CD73 polypeptide expression level in the firstbiological sample can be measured or estimated and compared to astandard CD73 polypeptide level, the standard being taken from a secondbiological sample obtained from an individual not having the disorder orbeing determined by averaging levels from a population of individualsnot having the disorder. As will be appreciated in the art, once the“standard” CD73 polypeptide level is known, it can be used repeatedly asa standard for comparison.

By “biological sample” is intended any biological sample obtained froman individual, cell line, tissue culture, or other source of cellspotentially expressing CD73. Methods for obtaining tissue biopsies andbody fluids from mammals are well known in the art.

IX. KITS COMPRISING CD73-BINDING MOLECULES

The present disclosure also provides kits that comprise at least one ofthe CD73-binding molecules described herein, e.g., anti-CD73 antibodiesor antigen-binding fragment thereof, variants, or derivatives of themolecules disclosed herein (e.g., a clone 10.3 antibody or a clone 2C5antibody), that can be used to perform the methods described herein. Incertain aspects, a kit comprises at least one purified anti-CD73antibody or an antigen-binding fragment thereof in one or morecontainers. In some aspects, the kits contain all of the componentsnecessary and/or sufficient to perform a detection assay, including allcontrols, directions for performing assays, and any necessary softwarefor analysis and presentation of results. One skilled in the art willreadily recognize that the disclosed CD73-binding molecule, e.g., ananti-CD73 antibody or antigen-binding fragment thereof of the presentdisclosure (e.g., a clone 10.3 antibody or a clone 2C5 antibody) can bereadily incorporated into one of the established kit formats which arewell known in the art.

X. IMMUNOASSAYS

Anti-CD73 binding molecules disclosed herein, e.g., anti-CD73 antibodiesor antigen-binding fragments thereof, variants, or derivatives of themolecules disclosed herein (e.g., a clone 10.3 antibody or a clone 2C5antibody), can be assayed for immunospecific binding by any method knownin the art. The immunoassays that can be used include but are notlimited to competitive and non-competitive assay systems usingtechniques such as Western blots, radioimmunoassays, ELISA (enzymelinked immunosorbent assay), “sandwich” immunoassays,immunoprecipitation assays, precipitin reactions, gel diffusionprecipitin reactions, immunodiffusion assays, agglutination assays,complement-fixation assays, immunoradiometric assays, fluorescentimmunoassays, protein A immunoassays, to name but a few. Such assays areroutine and well known in the art (see, e.g., Ausubel et al., eds,(1994) Current Protocols in Molecular Biology (John Wiley & Sons, Inc.,NY) Vol. 1, which is incorporated by reference herein in its entirety).

CD73-binding molecules, e.g., anti-CD73 antibodies or antigen-bindingfragments thereof, and their variants or derivatives (for example, aclone 10.3 antibody or a clone 2C5 antibody), can be employedhistologically, as in immunofluorescence, immunoelectron microscopy ornon-immunological assays, for in situ detection of CD73 or conservedvariants or peptide fragments thereof. In situ detection can beaccomplished by removing a histological specimen from a patient, andapplying thereto a labeled CD73-binding molecule, e.g., an anti-CD73antibody or antigen-binding fragment thereof, variant, or derivativethereof, preferably applied by overlaying the labeled CD73-bindingmolecule (e.g., and antibody or fragment) onto a biological sample.Through the use of such a procedure, it is possible to determine notonly the presence of CD73, or conserved variants or peptide fragments,but also its distribution in the examined tissue. Using the presentdisclosure, those of ordinary skill will readily perceive that any of awide variety of histological methods (such as staining procedures) canbe modified in order to achieve such in situ detection.

The binding activity of a given lot of CD73-binding molecule, e.g.,anti-CD73 antibody (for example, a clone 10.3 antibody or a clone 2C5antibody) or antigen-binding fragment thereof, variant, or derivativethereof can be determined according to well-known methods. Those skilledin the art will be able to determine operative and optimal assayconditions for each determination by employing routine experimentation.

Methods and reagents suitable for determination of bindingcharacteristics of an isolated CD73-binding molecule, e.g., anti-CD73antibody (for example, a clone 10.3 antibody or a clone 2C5 antibody) orantigen-binding fragment thereof, variant, or an altered/mutantderivative thereof, are known in the art and/or are commerciallyavailable. Equipment and software designed for such kinetic analyses arecommercially available (e.g., BIAcore, BIAevaluation software, GEHealthcare; KinExa Software, Sapidyne Instruments).

The practice of the present disclosure will employ, unless otherwiseindicated, conventional techniques of cell biology, cell culture,molecular biology, transgenic biology, microbiology, recombinant DNA,and immunology, which are within the skill of the art. Such techniquesare explained fully in the literature. See, for example, Sambrook etal., ed. (1989) Molecular Cloning A Laboratory Manual (2nd ed.; ColdSpring Harbor Laboratory Press); Sambrook et al., ed. (1992) MolecularCloning: A Laboratory Manual, (Cold Springs Harbor Laboratory, NY); D.N. Glover ed., (1985) DNA Cloning, Volumes I and II; Gait, ed. (1984)Oligonucleotide Synthesis; Mullis et al. U.S. Pat. No. 4,683,195; Hamesand Higgins, eds. (1984) Nucleic Acid Hybridization; Hames and Higgins,eds. (1984) Transcription And Translation; Freshney (1987) Culture OfAnimal Cells (Alan R. Liss, Inc.); Immobilized Cells And Enzymes (IRLPress) (1986); Perbal (1984) A Practical Guide To Molecular Cloning; thetreatise, Methods In Enzymology (Academic Press, Inc., N.Y.); Miller andCalos eds. (1987) Gene Transfer Vectors For Mammalian Cells, (ColdSpring Harbor Laboratory); Wu et al., eds., Methods In Enzymology, Vols.154 and 155; Mayer and Walker, eds. (1987) Immunochemical Methods InCell And Molecular Biology (Academic Press, London); Weir and Blackwell,eds., (1986) Handbook Of Experimental Immunology, Volumes I-IV;Manipulating the Mouse Embryo, Cold Spring Harbor Laboratory Press, ColdSpring Harbor, N.Y., (1986); and in Ausubel et al. (1989) CurrentProtocols in Molecular Biology (John Wiley and Sons, Baltimore, Md.).

General principles of antibody engineering are set forth in Borrebaeck,ed. (1995) Antibody Engineering (2nd ed.; Oxford Univ. Press). Generalprinciples of protein engineering are set forth in Rickwood et al., eds.(1995) Protein Engineering, A Practical Approach (IRL Press at OxfordUniv. Press, Oxford, Eng.). General principles of antibodies andantibody-hapten binding are set forth in: Nisonoff (1984) MolecularImmunology (2nd ed.; Sinauer Associates, Sunderland, Mass.); and Steward(1984) Antibodies, Their Structure and Function (Chapman and Hall, NewYork, N.Y.). Additionally, standard methods in immunology known in theart and not specifically described are generally followed as in CurrentProtocols in Immunology, John Wiley & Sons, New York; Stites et al.,eds. (1994) Basic and Clinical Immunology (8th ed; Appleton & Lange,Norwalk, Conn.) and Mishell and Shiigi (eds) (1980) Selected Methods inCellular Immunology (W.H. Freeman and Co., NY).

Standard reference works setting forth general principles of immunologyinclude Current Protocols in Immunology, John Wiley & Sons, New York;Klein (1982) J., Immunology: The Science of Self-Nonself Discrimination(John Wiley & Sons, NY); Kennett et al., eds. (1980) MonoclonalAntibodies, Hybridoma: A New Dimension in Biological Analyses (PlenumPress, NY); Campbell (1984) “Monoclonal Antibody Technology” inLaboratory Techniques in Biochemistry and Molecular Biology, ed. Burdenet al., (Elsevere, Amsterdam); Goldsby et al., eds. (2000) KubyImmunnology (4th ed.; H. Freemand & Co.); Roitt et al. (2001) Immunology(6th ed.; London: Mosby); Abbas et al. (2005) Cellular and MolecularImmunology (5th ed.; Elsevier Health Sciences Division); Kontermann andDubel (2001) Antibody Engineering (Springer Verlan); Sambrook andRussell (2001) Molecular Cloning: A Laboratory Manual (Cold SpringHarbor Press); Lewin (2003) Genes VIII (Prentice Hall2003); Harlow andLane (1988) Antibodies: A Laboratory Manual (Cold Spring Harbor Press);Dieffenbach and Dveksler (2003) PCR Primer (Cold Spring Harbor Press).

All of the references cited above, as well as all references citedherein, are incorporated herein by reference in their entireties.

The following examples are offered by way of illustration and not by wayof limitation.

EXAMPLES

Aspects of the present disclosure can be further defined by reference tothe following non-limiting examples, which describe in detailpreparation of certain antibodies of the present disclosure and methodsfor using antibodies of the present disclosure. It will be apparent tothose skilled in the art that many modifications, both to materials andmethods, can be practiced without departing from the scope of thepresent disclosure.

CD73 (Cluster of Differentiation 73), also known as ecto-5′-nucleotidase(NT5E), is a transmembrane receptor found on tumor cells as well as innormal stromal cells such as endothelial cells and certain leukocytes.CD73 catalyzes adenosine monophosphate to adenosine and organicphosphate. Binding of the extracellular portion of adenosine receptorssignals through cyclic AMP to inhibit T-cell receptor activation(reviewed by Linden and Cekic, 2012). CD73 is believed to play a role inmediating the inhibitory function of regulatory B and T lymphocytes(Saze et al, 2013), as well as in maintaining endothelial integrity(reviewed by Jalkanen and Salmi, 2008).

In addition to its role in normal biology, CD73 and adenosine affecttumor biology. The presence of extracellular adenosine within the tumormicroenvironment has been described as an immunosuppressive “halo”(Antonioli et al, 2013). Consistent with this role for adenosine,knockout mice lacking adenosine receptors have been shown to rejecttumors more readily than normal mice (Ohta et al, 2006). The primarysource of extracellular adenosine within tumors is believed to be CD73(Augusto et al, 2013). Consistent with this hypothesis as well asstudies with A2A deficient mice, knockout mice lacking CD73 haveincreased anti-tumor immunity (Stagg et al, 2011) and show decreasedcarcinogenesis (Stagg et al, 2012) when compared normal mice.Specifically, extracellular adenosine is believed to mediate theimmunosuppressive effects of both regulatory T cells and myeloid-derivedsuppressor cells (MDSCs), among others (reviewed by Antonioli et al,2013). Taken together with other studies showing that molecularinhibition of CD73 with small molecules or antibodies can inhibit tumorformation, growth, and metastasis (reviewed by Young et al, 2014), it ishypothesized that tumors use CD73 to generate adenosine and, thereby, tosuppress anti-tumor immunity. Accordingly, anti-CD73 antibodies thatselectively bind to and inhibit the ectonucleotidase activity of CD73are likely to be useful for enhancing an anti-tumor immune response.

Example 1 Isolation and Identification of Anti-CD73 Antibodies

Human scFv phage display libraries were panned with biotinylated CD73extracellular domain (ECD) to isolate antibodies binding to human,cynomolgus, and murine CD73. CD73-specific scFv antibodies were isolatedfrom the human scFv phage display library in a series of repeatedalternate selection cycles on biotinylated human and murine CD73extracellular domain (ECD) produced in-house from mammalian cellsessentially as described previously in Lloyd et al., PEDS 22:159-68(2009). ScFv genes from rounds 2 and 3 of the selection outputs wereconverted in batch into bacterial scFv-Fc or Fab expression vectors.Bacterial culture supernatants carrying soluble scFv-Fc or Fab werescreened for their binding to human, murine, and cynomolgus CD73 ECD byELISA or homogeneous time resolved fluorescence HTRF). The top hitsshowing cross reactivity were selected, subjected to DNA sequencing, andconverted to whole immunoglobulin G1 triple mutant antibody format(“IgG-TM”, IgG1 Fc sequence incorporating mutations L234F, L235E andP331S). IgG1 TM antibodies were expressed in mammalian cells, purifiedby affinity chromatography and ranked based on their characteristics inbinding and functional assays.

The lead antibody, CD730010, was shown to bind specifically to human,murine, and cynomolgus CD73-expressing cells (by flow cytometry), and toinhibit the activity of recombinant soluble CD73 ECD as well as nativeCD73 displayed on cells. Affinity maturation of CD730010 was initiatedto enhance binding affinity of CD730010 to human CD73.

Prior to affinity optimization, it was attempted to revert as manyframework residues of CD730010 to the closest human germline sequences(based on IMGT repertoire) without impairing affinity (See Example 8).This was done to minimize the potential immunogenicity of the finalantibody drug in humans. All framework residues of the VL domain and allexcept one framework residue of the VH domain could be reverted to matchthe amino sequence of human germlines IGLV1-44, IGLJ3, IGHV3-23, andIGHJ2. Lysine in position 94 (Kabat numbering; Kabat, 1991) of the VHdomain of CD730010 could not be reverted without loss of affinity.

TABLE 10 Affinity of parental anti-CD730010 antibody and antibodyvariants with germlined amino acids. amino acid in VH amino acid in VLposition position EC50 antibody variant 1 2 11 37 39 94 [nM] CD730010 LP V K V R 69 CD730010 GL9 Q S A Q L R 64 CD730010 GL10 L P V K V K 205CD730010 GL18 Q S A Q L K 132

The affinity and potency of germlined CD730010 antibody was enhanced bygenerating libraries of CDR variants and testing the variants forimproved binding to CD73 (See Example 9). Several mutations with thebest improvement in affinity were combined to generate the candidatedrug MEDI9447. The nucleotide and deduced amino acid sequences ofMEDI9447 are shown in FIGS. 1A-1D.

Example 2 Epitope Binning of Anti-CD73 Antibodies

The ability of anti-CD73 antibodies to compete with each other forbinding to human CD73 ECD was assessed on an Octet instrumentessentially as described (Abdiche Y N et al., Anal Biochem 386: 172-80(2009). CD73 ECD protein and first anti-CD73 antibody were pre-incubatedand added to a biotinylated second anti-CD73 antibody captured on aStreptavidin sensor. If the first anti-CD73 antibody blocked binding ofCD73 ECD to the second anti-CD73 antibody, both antibodies were placedin same or overlapping epitope bins. If both antibodies could bindsimultaneously to CD73 ECD, they were placed in non-overlapping epitopebins. Pairwise testing of the anti-CD73 antibodies demonstrated thatthey belong to 3 non-overlapping epitope bins (Table 2).

TABLE 2 Epitope bins of anti-CD73 antibodies Epitope bin Antibodies ACD730002, CD730004, CD730008, CD730011 B CD730003, CD730010, CD730021,CD730042, CD730046, CD730047 C CD730068, CD730069

Example 3 Binding of Anti-CD73 Antibodies to CD73

The binding affinity and specificity of anti-CD73 antibodies wasdetermined by Surface Plasmon Resonance (SPR) and flow cytometry.

A ProteOn XPR36 instrument was used to characterize binding of MEDI9447to human, murine, and cynomolgus CD73 ECD. MEDI9447 wasaffinity-captured using an anti-human Fc antibody. CD73 ECD was in themobile phase. The association and dissociation of CD73 to MEDI9447 couldbe accurately described with the Langmuir 1:1 model. The results shownin Table 3 demonstrate that the affinity of MEDI9447 to CD73 ECD fromthe three species is comparable and in the low picomolar range.

TABLE 3 Affinity of MEDI9447 to CD73 ECD Determined by Surface PlasmonResonance Analyte k_(a) (M⁻¹s⁻¹) k_(d) (s⁻¹) K_(D) (M) Human CD73 ECD2.57 × 10⁶ 1.06 × 10⁻⁵ 4.1 × 10⁻¹² Murine CD73 ECD 2.41 × 10⁶ 2.32 ×10⁻⁶ 0.9 × 10⁻¹² Cynomolgus CD73 2.71 × 10⁶ 1.76 × 10⁻⁵ 6.5 × 10⁻¹² ECDk_(a) Association rate constant; k_(d) Dissociation rate constant; K_(D)Dissocation constant

Binding of MEDI9447 to native CD73 expressed on human, murine, andcynomolgus monkey cell lines was characterized by flow cytometry. Thecells were incubated with various concentrations of MEDI9447 andantibody binding was monitored with and fluorophore-labeled anti-humanFc antibody. A plot of the median fluorescence intensity as a functionof the MEDI9447 concentration was fitted nonlinearly using a one-sitebinding isotherm model to calculate the equilibrium dissociationconstant. The analysis by flow cytometry confirms the binding ofMEDI9447 to human, murine, and cynomolgus CD73 with comparableaffinities (Table 4), although the K_(D) values are 13-126-fold greaterthan those determined by SPR, probably because of conformationaldifferences between recombinant and native CD73.

TABLE 4 Affinity of MEDI9447 to Native CD73 Determined by Flow CytometryAnalyte K_(D) (M) MDA-MB-231 cells (human) 154 × 10⁻¹² 4T1 cells(murine) 113 × 10⁻¹² MK-1 cells (cynomolgus)  84 × 10⁻¹²

To determine the specificity of MEDI9447 for human CD73 by flowcytometry, cell lines were developed. MDA-MB-231 cells, which are humanbreast cancer cells derived from a pleural effusion, were transfectedwith human CD73 short hairpin RNA (shRNA) to knock down the cell-surfaceexpression of CD73. Jurkat cells, a line of T cells derived from Burkittlymphoma cells, were transfected with a plasmid expressing human CD73mRNA to knock in cell-surface expression of CD73. Jurkat cells expresslittle endogenous CD73.

Specificity of MEDI9447 for human CD73 was determined by the ratio ofMEDI9447 binding to a high CD73-expressing cell line (MDA-MB-231) to lowexpressing cell line (MDA-MB-231, CD73-shRNA). Specificity of MEDI9447for human CD73 was also determined by the ratio of high CD73 expressingcell line (Jurkat-CD73 knock-in) to lower expressing cell line Jurkat.

Specificity of MEDI9447 for murine CD73 (mCD73) was determined by flowcytometry comparing the mouse cell line 4T1 (high mCD73 expression) tothe knocked-down cell line (4T1 mCD73-shRNA). In addition, specificityof MEDI9447 for Jurkat cells with murine CD73 knock-in was compared withwild-type Jurkat cells (no murine CD73).

TABLE 5 Specificity of MEDI9447for Human and Mouse CD73 Specificity MeanFluorescence of Intensity Ratio MEDI9447 Cell Line Relationship (MFIR)human MDA-MB-231/MDA-MB- 3.5 231(CD73- shRNA) human Jurkat (CD73knock-in)/Jurkat 7.9 Mouse 4T1/4T1(mCD73 -shRNA) 3.9 Mouse Jurkat (mCD73knock-in)/Jurkat 57.1

Example 4 Internalization of CD73 by Anti-CD73 Antibody MEDI9447

Antibody-mediated internalization or shedding of CD73 was assessed byflow cytometry. MDA-MB-231 cells were incubated in presence of 100 nMMEDI9447 or negative control antibody R347 in growth medium at 37° C.for 0-4 hours. Cells were washed and resuspended in ice-cold PBS. Thepresence of CD73 on the cell surface was detected by adding 10 nMDyLight488-labeled detection antibody. Cells were incubated for 15minutes, washed and analyzed by flow cytometry. The detection antibodybinds to an epitope of CD73 that is different from the MEDI9447 epitopeand both antibodies simultaneously bind to CD73 without interference.Cell surface expression of CD73 dropped to 73% of its original valueafter 4 hours incubation with MEDI9447, suggesting that 27% of CD73 waseither internalized or shed upon MEDI9447 binding (Table 6).

TABLE 6 Percentage of CD73 remaining on the cell surface of MDA-MB-231cells after incubation with test antibody Time [h] R347 MEDI9447 0 100%100%  0.25 107% 90% 0.5 104% 90% 1 102% 87% 2 104% 80% 4 102% 73%

Internalization of MEDI9447 into cell lines MDA-MB-231 (human mammarycarcinoma) and 4T1 (murine mammary carcinoma) was assessed using a humanAntibody Internalization Kit that is sold commercially as the FabZAPassay (Advanced Targeting Systems, San Diego Calif.). Serial dilutionsof MEDI9447 or negative control antibody R347 were pre-incubated with 40nM FabZAP reagent (Fab fragment of a polyclonal anti-human IgG antibodyconjugated to the cytotoxic protein saporin) and then added to the celllines. After 3 days in culture, cell proliferation was measured using aluminescent cell viability assay sold commercially as the CellTiter-Gloassay (Promega, Madison Wis.). This assay was used to calculate EC₅₀values and maximum toxicity. The FabZAP reagent cannot internalize intocells on its own. It binds to a test antibody (e.g., MEDI9447) and iscytotoxic only upon internalization of the test antibody. MEDI9447caused internalization of FabZAP and inhibited cell proliferation in adose-dependent manner.

TABLE 7 Antibody-mediated Internalization of Cytotoxic FabZAP Reagentinto MDA-MB-231 Cells and 4T1 Cells MDA-MB-231 4T1 EC₅₀ maximum EC₅₀maximum [pM] toxicity [pM] toxicity MEDI9447 3.5 97% 18.5 97%

Cell proliferation of MDA-MB-231 cells and 4T1 cells treated with serialdilutions of test antibody and FabZAP reagent was measured byCellTiter-Glo assay (FIG. 2). The signal from the negative controlantibody R347 in the CellTiter-Glo assay was subtracted from the signalof MEDI9447 and the EC50 value and maximum toxicity were calculated byfitting the dose-response curve using non-linear regression analysis.

Example 5 Inhibition of 5′Ectonucleotidase Activity by Anti-CD73Antibody MEDI9447

In this study, the functional activity of MEDI9447 was determined in anin vitro assay that measured the CD73-catalyzed hydrolysis of AMP usinga human non-small cell carcinoma cell line, NCI-H322. Formulation ofMEDI9447 was prepared by diluting its stock solution in serum-free RPMImedium to a final concentration of 1 μM. Formulation of R347 wasprepared by diluting its stock solution in RPMI to a final concentrationof 1 μM.

NCI-H322 cells were centrifuged for 5 minutes at 1500 rpm. Thesupernatant was removed and replaced with serum-free RPMI medium. Thecell suspension was counted using the ViCell (Beckman, Coulter) cellcounter. The cells were plated into 96-well plates at a cell density of10,000 cells per 100 μLs per well. 50 μL of 4× concentrated AMP (200 μM)was added. The plates were then incubated at 37° C., 5% CO₂ for 24hours. Plates were centrifuged and 50 μL of the culture supernatant wastransferred well-to-well to 96-well opaque round bottom plates. 2×ATPwas then added. CellTiterGlo® (Promega) was added according to themanufacturer's instructions. Cellular enzyme inhibition of 5′ectonucleotidase was measured on a multilabel reader, the Perkin-ElmerEnvision Workstation. The samples were analyzed using Prism Software.

MEDI9447 specifically inhibited dephosphorylation of adenosinemonophosphate (AMP) in a human in vitro system. In a cell-based assay ofsurface-expressed CD73, conversion of adenosine monophosphate toadenosine was reduced in a dose-dependent manner by MEDI9447, but not byan irrelevant isotype control antibody (FIG. 3). The results depicted inFIG. 3 were obtained using CD73-expressing NSCLC cells that were platedinto 96-well non-tissue culture treated plates (Falcon 3788) at 10,000cells per well in 100 μL of RPMI medium without additives. Antibodieswere added in duplicate along with AMP (200 μM final concentration) andplates were incubated at 37° C., 5% CO₂ for 24 hours. Plates were thencentrifuged for 3 minutes at 1500 rpm. Supernatants were collected intoa new 96 well plate (Costar #3605) and ATP was added to a finalconcentration of 100 μM. CellTiter-Glo® reagent (Promega) was added 1:1and cellular CD73 enzyme AMP phosphorylase activity was determined bymeasuring ATP levels using the Envision luminescence plate reader(Perkin Elmer). Buffer containing only ATP and AMP was used as anegative control. The assay was repeated and the results shown at FIG. 3are representative of two similar experiments using other human cancercell lines.

These results indicate that MEDI9447 inhibited the production ofadenosine by cancer cells. Adenosine mediates the tumor'simmunosuppressive effects within the tumor microenvironment.

Example 6 Reduction in Tumor-Infiltrating Myeloid-Derived SuppressorCells by MEDI9447

CT26 cells, which are derived from a murine colon cancer, wereestablished by subcutaneous (SC) injection of 5×10⁵ cells suspended in0.1 mL of PBS into the right flanks of 4-to-6-week-old female mice. Themice were treated with MEDI9447 or with a control antibody.

10 mice per group were used in this study. Animals were randomlyassigned into groups. Animals in Group 1 were untreated and Group 2 wasadministered an isotype control. MEDI9447 was administered to Group 3.Test articles were administered intraperitoneally twice weekly startingon Day 3. On Day 16, 5 animals from each group were necropsied andtumors were isolated.

Group designation and dose levels are presented in Table 8.

TABLE 8 Group Designation and Dose Levels Number of animals Days of Doselevel Group (female) Treatment dosing (mg/kg) ^(a) ROA 1 5 untreated N/AN/A N/A 2 5 isotype 2X weekly 20 mg/kg IP 3 5 MEDI9447 2X weekly 10mg/kg IP N/A = not applicable; ROA = route of administration.Tumors were measured on Days 1, 7, 9, 12, 14, and 16 by caliper, and thevolumes of tumors were calculated as follows:

(tumor volume length (mm)×(tumor volume width)² (mm))/2  (1)

The anticancer effects of MEDI9447 were expressed as percent tumorgrowth inhibition, which was calculated as follows:

(Average tumor volume for MEDI9447/Average tumor volume forR347-TM)×100  (2)

Tumors were isolated for flow cytometry. Tumors were dissected from CT26tumor-bearing mice on study Day 16. Tumors were cut into small piecesand were digested with collagenase. After a 30-minute incubation, thedigested sample was passed through a 70-micron filter. Dissociated cellswere pelleted at 1000 rpm for 5 minutes at 4° C. and were resuspended influorescence-activated cell sorting (FACS) buffer. Cells were counted onViCell using the default setting. 1×10⁶ cells were plated per well.Cells were stained with anti-CD45 (to detect all leukocytes) anti-GR1(to detect MDSCs) and anti-Ly6g (Gran MDSC). Data were acquired on theLSRII flow cytometer. Significant p-values, if any, obtained from theMDSC analyses are presented in FIG. 4 adjacent to the descriptivestatistics (ie, mean and standard deviation).

MEDI9447 inhibited tumor growth in murine CT26 syngeneic Balb/C tumormodel (FIG. 4).

MEDI9447 reduced the proportion of tumor-infiltrating MDSCs in themurine CT26 syngeneic Balb/C tumor model (FIG. 5).

MEDI9447 inhibited the growth of CT26 murine syngeneic tumors. Inaddition, myeloid-derived suppressor cells were decreased in syngeneicCT26 colon carcinoma tumors following treatment with MEDI9447.Intra-tumoral MDSCs have an immunosuppressive effect on the tumormicroenvironment, allowing for enhanced tumor growth. The observedreduction in intra-tumoral MDSCs following treatment with MEDI9447demonstrates a mechanism by which treatment with MEDI9447 reduces tumorimmune suppression.

Example 7 A Combination of MEDI9447 mIgG1 and an Anti-PD-1 AntibodyReduced Tumor Growth and Increased Survival

Syngeneic tumors were established by subcutaneous (SC) injection of 0.1ml of 5×10⁶ CT26 cells/ml suspended in HBSS into the right flanks of 8-to 10-week-old animals. Tumors were measured by caliper and the volumesof tumors (TV) were calculated using the following formula:

TV=(L×W ²)/2  (1)

where L is tumor length in millimeters and W is tumor width is inmillimeters

Mice were randomized into groups based on bodyweight. There were noanimal substitutions. 60 female Balb/c mice were used in this study.

Animals were randomly assigned into 6 groups. Animals were administeredMEDI9447(mIgG1). Test articles were administered by intraperitoneal (IP)injection twice weekly starting on Day 3. Group designation and doselevels are presented in Table 9.

TABLE 9 Group Designation and Dose Levels Number of Schedule animals ofdosing Dose level Group (Female) Treatment (2x weeky) (mg/kg) ^(a) ROA 110 Untreated NA NA NA 2 10 Isotype 4 doses 10 ip mIgG1 3 10 Isotype 4doses 10 ip rIgG2a 4 10 MEDI9447 4 doses 10 ip mIgG1 6 10 Anti-PD1 4doses   0.5 ip 7 10 Anti-PD1 + 4 doses 0.5 + 10 ip MEDI9447 F = female;IV = intravenous; M = male; ROA = route of administration. ^(a) Dosevolume: 10 mL/kg.

(a) Results of In Vivo Tumor Inhibition Study

CT26 murine colon carcinoma were implanted into syngeneic Balb/C miceand treated with anti-CD73 (MEDI9447 mIgG1; 10 mg/kg), anti-PD1 (0.5mg/kg) or the combination (10 mg/kg anti-CD73 and 0.5 mg/kg anti-PD1).The combination treatment significantly inhibited tumor growth whencompared to anti-CD73 alone (p=0.015, ANOVA). Tumor volumes from eachgroup of animals were plotted for individual animals out to study day40. No control group mice were tumor free by the end of the 40 day studyperiod (See FIG. 6). Anti-CD73 treatment alone resulted in 10% tumorfree animals at the end of study. Anti-PD1 treatment alone also resultedin 10% tumor free animals at the end of study. Remarkably, thecombination of anti-CD73 and anti-PD treatment resulted in 60% tumorfree mice. None of the control group mice were tumor free by the end ofthe study. CT26 tumors were measured in mice treated with anti-CD73(MEDI9447 mIgG1), anti-PD1 or the combination of anti-CD73 and anti-PD1.Mice were measured until study day 40, and humanely sacrificed oncetumors reached 2000 mm³. The combination of anti-CD73 and anti-PD1treatment together resulted in a statistically significant increase insurvival when compared to anti-CD73 or anti-PD1 treatment alone (pvalue=0.005 and p=0.038, respectively, Log Rank Test) (FIG. 7). Mediansurvival increased from 25 and 33 days (anti-CD73 and anti-PD1,respectively) compared to “undefined” at day 40 for the combination.

TABLE 9 Outcome at Study Day 40 Tumor free mice Survival Treatment (%)(%) untreated 0 0 Isotype mIgG1 0 0 Isotype rIgG2a 0 0 Anti-CD73 10 10Anti-PD1 10 20 Anti-CD73 + Anti-PD1 60 70

In summary, anti-CD73 antibody, MEDI9447 mIgG1, showed enhancedanti-tumor activity when combined with an anti-PD-1 antibody in a murinesyngeneic CT26 colon carcinoma model. In addition, the combination ofanti-CD73 and anti-PD treatment resulted in 60% tumor free mice. Thecombination of anti-CD73 and anti-PD1 treatment together also resultedin a statistically significant increase in survival when compared toanti-CD73 or anti-PD1 treatment alone.

Example 8 Anti-CD730010 Antibody and Antibody Variants

The VH and VL amino acid sequences of CD730002 and CD730010 were alignedto the known human germline sequences using IMGT/V-QUEST(http://www.imgt.org) and the closest germline sequences were identifiedby sequence similarity. For the CD730010 VH domain, these were IGHV3-23and IGHJ2. For the CD730010 VL domain, these were IGLV1-44 and IGLJ3.Six non-germline residues outside the CDR regions were identified: R94in VH, and L1, P2, V11, K37, and V39 in VL (Kabat numbering).Nucleotides in the CD730010 IgG1-TM expression vector were back-mutatedby standard molecular biology techniques, so that the resultingexpression vectors encoded germline amino acids in these positions (K94in VH, and Q1, S2, All, Q37, and L39 in VL). The CD730010 IgG1-TMprotein variants were expressed, purified and tested for binding toCD73-expressing MD-MB-231 cells by flow cytometry. All 5 non-germlineamino acids in VL could be changed to their germline residues withoutimpairing binding. However, R94 in VH is important for binding andchanging it to K impairs binding. The nucleotide sequence of CD730010GL9 was used as template for generating affinity-optimized antibodyvariants.

For CD730002, the closest germline genes were IGHV3-23 and IGHJ3 for theVH domain, and IGLV3-1 and IGLJ3 for the VL domain. Four non-germlineresidues outside the CDR regions were identified: R94 in VH, and T20,R57, L81 and F87 in VL (Kabat numbering). Nucleotides in the CD730002IgG1-TM expression vector were back-mutated by standard molecularbiology techniques, so that the resulting expression vectors encodedgermline amino acids in these positions (K94 in VH, and S20, G57, M81,and Y87 in VL). The CD730002 IgG1-TM protein variants were expressed,purified and tested for binding to recombinant human and murine CD73 byflow cytrometry. All 4 non-germline amino acids in VL could be changedto their germline residues without impairing binding. However, R94 in VHis important for binding and changing it to K impairs binding. VariantCD730002 SGMY (non-germlined V, fully germlined VL) was used as atemplate for generating affinity-optimized antibody variants.

Example 9 Affinity-Optimization of Anti-CD73 Antibodies CD730010GL9

CD730010GL9 IgG1-TM was enhanced by screening Fab libraries comprisingvariant CDR sequences with single amino acid mutations. Each of the 61positions in the six CDRs was individually randomized to 19 amino acids(all natural amino acids except Cysteine), generating a library with atheoretical diversity of 1159 unique clones (19 amino acids per positiontimes 61 positions). Bacterial Fab fragments were produced from 4224clones of the library and screened for binding to human and murine CD73protein by capture ELISA (Assay 2). 180 clones with increased bindingsignal compared to parental CD730010 GL9 IgG1-TM were selected and themutations in the VH or VL domain were identified by DNA sequencing. TheFab concentration in the bacterial supernatants was normalized and thebinding of the normalized supernatants to human and murine CD73 proteinwas evaluated by direct ELISA (Assay 1). Table 11 lists selectedbeneficial single amino acid substitutions and their effect on bindingto recombinant CD73 protein.

TABLE 11 Single amino acid variants of CD730010 GL9 with improvedaffinity. ELISA signal, fold improvement Amino acid over parentalantibody CDR change huCD73 muCD73 L1 P32E 27.7 6.7 L1 P32D 11.7 6.5 H3Y102K 9.9 7.4 L2 N51D 8.9 4.5 H2 G54N 8.9 7.1 H2 S52W 8.9 4.4 H3 Y102M7.9 6.3 H3 Y102L 7.3 5.8 L2 S56G 7.1 5.6 L2 N51A 6.7 2.5 H3 Y102A 6.65.0 L1 P32G 6.1 5.8 L1 P32A 6.0 5.5 L2 Q53L 6.0 3.8 L2 Q53Y 5.8 2.3 L2P55L 5.7 4.3 H2 S56R 5.6 4.9 L2 N51Q 4.2 2.3 H2 G54W 4.2 3.7 H2 A50L 4.23.0 L2 Q53F 4.1 2.7 H1 M34Y 3.9 2.9 L2 P55I 3.7 3.2 H3 Y102Q 3.6 3.0 L2Q53W 3.1 2.7 L2 Q53H 2.4 1.9 L2 L50F 2.2 1.4 H1 S35H 1.8 1.1 H1 M34I 1.51.1

To further improve the affinity of the anti-CD73 antibody, severalsingle amino acid changes which improved binding when compared toparental CD730010 GL9 were combined to create a combinatorial Fablibrary (Assay 4). Fab fragments of 4224 clones of the combinatoriallibrary were produced in E. coli and screened for binding to human andmurine CD73 protein by capture ELISA. The top 20 clones from eachscreening assay were selected for further characterization. The Fabconcentration in the supernatants was normalized and serial dilutions ofnormalized supernatants were tested for binding to human and murine CD73by capture ELISA and direct ELISA. Clones C1, C2, D3 and G10 showedstrong binding to human and murine CD73 and were selected for furthercharacterization.

Antigen-binding of CD730010 GL9 was also enhanced using affinity-basedphage selections. Large scFv libraries derived from the lead CD730010GL9 sequence were created by oligonucleotide-directed mutagenesis of thevariable heavy (VH) complementarity determining region 3 (CDR3) orvariable light (VL) chain CDR3 using standard molecular biologytechniques as described (Finch et al., JMB 411, 791-807 (2011)). Thelibraries were panned in a series of repeated alternate selection cycleswith biotinylated human and murine CD73 extracellular domain protein.ScFv genes from round 3 of the selection output were batch-convertedinto a bacterial IgG expression vector. Bacterial culture supernatantscontaining soluble IgG were screened for their binding to human andmurine CD73. IgG variants with significantly improved binding to CD73compared to parental CD730010 GL9 were subjected to DNA sequencing. Twovariants, GRVE and HPT, were selected for further characterization.

To generate further affinity improvements, beneficial mutationsidentified from the combinatorial Fab library and from theaffinity-based phage selection were combined creating variants 73combo1to 73combo6.

Example 10 Affinity-Optimization of Anti-CD73 Antibodies CD730002SGMY

CD730002SGMY IgG1-TM was enhanced by screening Fab libraries comprisingvariant CDR sequences with single amino acid mutations as described forCD730010GL9. Five amino acid mutations in the VH domain and four aminoacid mutations in the VL domain were identified that resulted inincreased binding signal to recombinant CD73. Table 12 lists beneficialsingle amino acid substitutions and their effect on binding torecombinant CD73.

TABLE 12 Single amino acid variants of CD730002SGMY with improvedaffinity. FACS signal, fold improvement Amino acid over parentalantibody CDR change MDA-MB-231 cells H1 Y32V 1.2 H1 M34R 1.1 H2 T57P 1.5H2 A60G 1.3 H2 G65R 1.3 L2 T52S 1.5 L2 R54Y 1.2 L2 P55L 1.9 L2 P55H 1.5

To further improve the affinity of the anti-CD73 antibody CD730002SGMY,IgG variants were prepared that harbored one beneficial amino acidchange in the VH domain and one beneficial amino acid change in the VLdomain. Antibody variants were prepared by transient transfection of293F cells and were screened for binding to MDA-MB-231 cells by flowcytometry. Clone 2C5 had a 3-fold lower EC50 value than parentalCD730002SGMY.

Example 11 Affinity of Enhanced Anti-CD73 Antibodies

The affinity of enhanced anti-CD73 antibodies (in IgG1-TM format) tohuman, murine, and cynomolgus CD73 was determined by flow cytometry andsurface plasmon resonsance (SPR) (Table 13). The enhanced antibodies hadpM affinity to cellular and recombinant CD73 from the three species.

TABLE 13 Affinity of anti-CD73 antibodies to human, murine, andcynomolgus CD73 KD [pM] flow cytometry MB- SPR (Proteon) MDA-231 4T1MK-1 human murine cyno (human) (murine) (cyno) CD73 CD73 CD73 CD7300108000 6100 ND 3580 2470 1920 CD730010GL9 8949 16365 16460 1640 ND ND P32E178 145 110 63 35 27 C1 179 95 160 29 6 12 C2 158 67 105 23 G10 354 259258 9 HPT 739 5812 1138 548 GRVE 125 88 101 29 73combo1 157 150 90 7 2 8(C1 + GRVE + HPT) 73combo2 166 64 74 5 (C2 + GRVE + HPT) 73combo3 154113 84 4 1 7 (D3 + GRVE + HPT) 73combo5 169 205 78 7 (G10 + GRVE + HPT)73combo6 166 82 107 15 (GRVE + HPT) CD730002 52 50 52 7 40 15 CD7300022C5 84 55 63 9 22 9

Example 12 The Anti-Human CD73 Antibody, Phen0203 hIgG1, InhibitedAMP-Mediated Suppression of CD4+CD25-T Cell Proliferation In Vitro, in aConcentration Dependent-Manner

A study was conducted to determine the ability of an anti-CD73 antibody(Phen0203) to relieve AMP-mediated T-cell suppression in vitro. In thisin vitro study, the ability of an anti-human CD73 antibody (Phen0203hIgG1) to inhibit the catalysis of adenosine monophosphate to adenosineand organic phosphate by CD73 and the subsequent impact on T-cellfunction was examined. Phen0203 hIgG1 has similar functional propertiesto MEDI9447, including the ability to inhibit the cellular andbiochemical enzymatic activity of CD73 in vitro).

Phen0203 hIgG1 antibody is a human IgG1 mAb with no engineering in theheavy chain constant region. Similar to MEDI9447, it also selectivelybinds to and inhibits production of immunosuppressive adenosine by theectonucleotidase activity of human CD73. However, Phen0203 lackscross-reactivity against mouse CD73.

In an assay for AMP-mediated T-cell suppression, primary human CD4⁺ Tcells depleted of CD25⁺ cells were isolated from the content ofleukocyte cones and used as effector cells; each cone was processedseparately. Briefly, the content from a leukocyte cone was diluted inPBS, then layered over Ficoll-Paque Plus (GE Healthcare, Chalfont StGiles, UK) and centrifuged at 400×g for 40 minutes with brakes turnedoff. Peripheral blood mononuclear cells (PBMC) were then isolated fromthe interface and washed with PBS by centrifugation at 200×g for 10minutes. Supernatant was discarded and cells were suspended in PBS.Viable cells were determined, then pelleted at 350×g for 5 minutes andsuspended in Robosep buffer (Stem Cell, Grenoble, France) at aconcentration of 5×10⁷ per mL. CD4⁺ T cells were isolated from PBMCs bynegative selection using the EasySep human CD4⁺ T cell enrichment kit(Stem Cell, Grenoble, France) and the RoboSep (Stem Cell, Grenoble,France). Purified CD4⁺ T cells were pelleted and resuspended at 1.5×10⁷per mL in Robosep buffer. Dynabeads CD25 (a component of DynabeadsRegulatory CD4⁺CD25⁺ T cell kit; Life Technologies, Paisley, UK) wereadded at 200 μL per 1.5×10⁷ cells and incubated for 25 minutes at 4° C.with continuous mixing. Cells were then placed into a DynaMag-15 magnet(Life Technologies, Paisley, UK) for 1 minute and the supernatantcontaining the CD4⁺CD25⁻ effector cells were transferred into a newtube.

Isolated effector cells were labeled with CFSE probe (3 μM) using theCellTrace CFSE cell proliferation kit (Life Technologies, Paisley, UK)at a cell density of 1×10⁶ cells per mL in PBS containing 0.1% BSA withan incubation period of 15 minutes at 37° C. Cells were washed twicewith warm X-Vivo 15 media and suspended at 5×10⁵ cells per mL in thesame media. Labeled effector cells were activated for 1 hour at 37° C.by adding 25 μL of anti-CD3 and anti-CD28 coated microbeads (Dynabeadshuman T-activator CD3/CD28; Life Technologies, Paisley, UK) per 1×10⁶cells and 60 IU/mL of rhIL-2. Thereafter, activated CD4+CD25-cells(approximately 50,000 in 100 μL) were added to wells of sterileround-bottom 96-well plates. Serial dilutions of the following reagentswere performed in X-Vivo 15 media (Lonza, Slough, UK): the test articlePhen0203 hIgG1; R347 control antibody; APCP as a positive control; andSCH58261 a selective antagonist for adenosine receptor A2A. Phen0203hIgG1 was received as a ready-to-use formulation (MedImmune,Gaithersburg, Md.) and was diluted in phosphate-buffered saline (PBS).R347 was received as a ready-to-use formulation (MedImmune,Gaithersburg, Md.) and was diluted in PBS.

To the cells in the plate, 50 μL of diluted reagents were added followedby 50 μL of X-Vivo 15 (Lonza, Slough, UK) containing 400 μM or 800 μM ofAMP (Sigma-Aldrich, Gillingham, UK). The following control wells werealso included: activated CFSE-labeled CD4⁺CD25⁻ cells with no AMP(activated control); CFSE-labeled CD4⁺CD25⁻ cells with AMP but notest/control articles (untreated control); and un-activated (restingcontrol) CFSE-labeled CD4⁺CD25⁻ cells with no AMP. Cells in the assaywere gently pelleted by centrifugation, at 100×g for 2 minutes, andplaced in a 37° C. humidified tissue culture incubator with 5% CO₂ for72 hours.

After 72 hours of incubation, cells were pelleted by centrifugation at380 g for 4 minutes, washed once with 100 μL of FACS buffer(eBioscience, Hatfield, UK) and finally suspended in 100 μL of PBScontaining 3.7% of formaldehyde for flow cytometry analysis on a BDFACSCanto II (BD Biosciences, Oxford, UK). Resting CFSE⁺CD4⁺CD25⁻ cellswith no AMP well was used to identify cells that have undergone cellulardivision (divided cells).

CD73 was found to be expressed on a subset of CD4⁺ T cells. In thepresence of extracellular AMP, CD73⁺ T cells have the potential toenable paracrine/autocrine pathways which involves the metabolism of AMPto adenosine by CD73, followed by the activation of the adenosinereceptors and the subsequent regulation of T cell function. ThisCD73/adenosine pathway was modeled in vitro by using purified CD4⁺CD25⁻primary human T cells activated by TCR-signaling and rhIL-2. T-cellproliferation was suppressed in the presence of 100 or 200 μM ofextracellular AMP.

The in vitro capacity for an anti-CD73 antibody (Phen0203 hIgG1) toinhibit AMP-mediated T cell suppression was evaluated. Addition ofPhen0203 hIgG1, in the presence of AMP, increased T cell proliferationin a concentration-dependent manner (FIG. 9). In contrast, R347 isotypecontrol antibody had no effect. Without intending to be bound by theory,this indicates that the binding of an anti-CD73 antibody to CD73 wasable to block or decrease the generation of adenosine and the subsequentinhibitory effect on T cell function via adenosine receptor signaling.

APCP and SCH58261 are known small molecule inhibitors of CD73 (Hausleret al., Cancer Immunol Immunother. 2011 60(10):1405-18) and adenosinereceptor A2A (Marcoli et al., Neuropharmacology 2003 45(2):201-10),respectively. The addition of these molecules also resulted in theincrease of T-cell proliferation in the presence of AMP (FIGS. 9 and10). Without intending to be bound by theory, this indicates a role forCD73, adenosine and adenosine receptor A2A signaling in mediating T-cellsuppression in this in vitro primary human cell assay system.

Phen0203 hIgG1, an anti-human CD73 antibody, was capable of inhibitingAMP-mediated suppression of CD4⁺CD25⁻ T cell proliferation in vitro, ina concentration dependent-manner. The data provide a scientificrationale for an anti-CD73 antibody approach targeting theimmunosuppressive effects of the AMP/CD73/adenosine pathway.

Example 13 A Combination of Anti-CD73 Antibody and Adenosine ReceptorInhibitor Had Synergistic Effects on TNF-Alpha Secretion

Studies have shown that molecular inhibition of CD73 and its productionof adenosine using anti-CD73 antibodies can inhibit tumor formation,growth, and metastasis. Adenosine receptor A2A is hypothesized to play arole in negatively regulating immune cells. Thus, the antitumor effectof anti-CD73 antibody, MEDI9447 (mIgG1), could be increased byadministering it in combination with an adenosine receptor inhibitor(A2ARi) was examined.

The release of immune activating cytokines IFNγ and TNFα was evaluatedin human mixed leukocyte cultures with anti-CD73 monoclonal antibodyalone and in combination with an adenosine receptor inhibitor (A2ARi).The levels of IFNγ and TNFα in supernatants were detected by ELISA.Human peripheral blood lymphocytes were set up in a mixed leukocytereaction for 72 hours and stimulated with anti-CD73 alone, A2ARinhibitor alone or both agents. Peripheral blood mononuclear cells frompairwise combinations of 8 donors were incubated for 72 hours in thepresence of 1 μM anti-CD73 antibody MEDI9447 and 1 μM A2ARi SCH58261,either alone or in combination. After incubation, supernatant levels ofInterferon gamma (IFNγ) and Tumor Necrosis Factor Alpha (TNFα) weremeasured using a Mesoscale ELISA plate. The levels of IFNγ and TNFαobserved after incubation with each compound were plotted as duplicatefold-control values using levels from incubation with an isotype controlantibody as a negative control.

The anti-CD73 antibody MEDI9447 (mIgG1) and adenosine receptor inhibitor(A2ARi) were capable of inducing these cytokines to different extents inhuman cells, as varying levels of IFNγ and TNFα were detected in thesupernatants (FIGS. 11 and 12). Anti-CD73 antibody, MEDI9447 (mIgG1),when combined with an adenosine receptor inhibitor (A2ARi), demonstratedenhanced TNFα levels in the in vitro human mixed lymphocyte stimulationassay across all donor pairs tested (FIG. 12). Indeed, administration ofthe combination of MEDI9447 and SCH58261 showed a synergistic effect onTNFα secretion in the human mixed lymphocyte stimulation assay in alldonor pairs.

Example 15 Methods and Assays Used

The following assays and methods were used to perform the precedingexamples.

Assay 1: Direct ELISA

384-well ELISA plates were coated with about 1.5 ng/well recombinantCD73 protein, blocked with 1% BSA/0.1% Tween20/PBS and incubating withantibody samples for 90 minutes at room temperature. This was followedby incubation with goat-anti-Iglambda-horseradish peroxidase (HRP)conjugate for 30 min at room temperature. HRP activity was detected withtetra methyl benzidine (TMB) substrate and the reaction was stopped with1 M HCl. Plates were read at 450 nm.

Assay 2: Capture ELISA

384-well ELISA plates were coated with about 3 ng/well sheep-anti-humanFd antibody (for screening antibodies in Fab format), blocked with 1%BSA/0.1% Tween20/PBS and incubating with samples for 90 minutes at roomtemperature. Biotinylated CD73 protein was then added for 1 h at roomtemperature. This was followed by incubation withstreptavidin-horseradish peroxidase (HRP) conjugate for 30 min at roomtemperature. HRP activity was detected with tetra methyl benzidine (TMB)substrate and the reaction was stopped with 1 M HCl. Plates were read at450 nm.

About 50 ng/well biotinylated recombinan CD73 was used to screen cloneswith single amino acid mutations. For the screening of clones from thecombinatorial library, 10 ng/well biotinylated recombinant CD73 wereused.

Assay 3: Flow Cytometry Binding Assay

All flow cytometry experiments were run at 4 C and reagents wereprepared in PBS/1% FBS buffer. 10,000 cells were incubated with testantibody in 50 uL volume for 4 hours. Cells were washed twice andincubated in 50 uL goat anti-human IgGFc-AlexaFluor647 conjugate for 15minutes. Cells were washed, resuspended in buffer supplemented withDapi, and analyzed on a flow cytometer. Dead cells, identified by highDapi staining, were excluded from the analysis. For the determination ofKD values, a plot of the median fluorescence intensity as a function oftest antibody concentration was fitted nonlinearly using a one sitebinding isotherm model.

Assay 4: Generation of the Antibody Library with Single Amino AcidChanges

Site-directed mutagenesis of the CDR codons of CD730010 or CD730002 wasperformed using a QuikChange Lightning Multi Site-Directed MutagenesisKit (Agilent) and primers. Each codon was mutagenized with a primerwhich replaced the wild-type codon with codon NNS. Mutagenized VH and VLgenes were cloned into a Fab vector for bacterial expression. E. colistrain BL21(DE3) was transformed with the antibody library, individualcolonies were picked and cultured in Magic Media (Invitrogen) for 24hours at room temperature to produce bacterial Fab fragments. Bacterialsupernatant was prepared and used to screen the antibody library inELISA binding assays.

Assay 5: Generation of the Antibody Library with Combinatorial AminoAcid Changes

CD730010GL9 VH and VL genes were cloned into a vector for bacterial Fabexpression. Site-directed mutagenesis of the CDR codons of CD730010GL9was performed using either QuikChange Lightning Multi Site-DirectedMutagenesis Kit (Agilent) or overlapping PCR and degenerate primers. Thedegenerate primers were designed to encode selected amino acid changesas well as the parental amino acid at the same position. E. coli strainBL21(DE3) was transformed with the Fab library, individual colonies werecultured in Magic Media (Invitrogen) for 24 hours at room temperature toproduce bacterial Fab fragments. Bacterial supernatants were used toscreen the antibody library in ELISA binding assays.

Assay 6: FabZAP Assay

1,000 cells/well were cultured in 96 well plates in RPMI/10% FBS. Serialdilutions of anti-CD73 antibodies starting at 5 nM were mixed withFabZAP reagent (Advanced Targeting Systems, San Diego Calif.) and addedto the cells. After 3 days incubation at 37 C, the cell proliferationwas measured using the CellTiter-Glo assay (Promega, Madison Wis.).

The preceding description of the specific aspects will so fully revealthe general nature of the invention that others can, by applyingknowledge within the skill of the art, readily modify and/or adapt forvarious applications such specific aspects, without undueexperimentation, without departing from the general concept of thepresent invention. Therefore, such adaptations and modifications areintended to be within the meaning and range of equivalents of thedisclosed aspects, based on the teaching and guidance presented herein.It is to be understood that the phraseology or terminology herein is forthe purpose of description and not of limitation, such that theterminology or phraseology of the present specification is to beinterpreted by the skilled artisan in light of the teachings andguidance.

SEQUENCE LISTING CD730002 VL >SEQ ID NO: 1QSVLTQPPSVSVSPGQTATITCSGDKVGDKYASWYQQKPGQSPVLVIYEDTKRPSRIPERFSGSNSGNTATLTISGTQALDEADYFCQAWDTSFWVFGGGTKLTVL CD730002 VH >SEQ ID NO: 2EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSCD730010 VL >SEQ ID NO: 3LPVLTQPPSVSGTPGQRVTISCSGSLSNIGRNPVNWYKQVPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLNGWLFGGGTKLTVLCD730010 VH >SEQ ID NO: 4EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDYWGRGTLVTVSSCD730011 VL >SEQ ID NO: 5NFMLTQPHSVSESPGKTVTISCTRSSGSIASKYVQWYQQRPGSSPMAVIYKDNQRSSGVPDRFSGSIDSSSNSASLTISGLKPEDEADYYCQSYDASNYYVFGTGTKVTVLCD730011 VH >SEQ ID NO: 6EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARRGHGLYFDLWGQGTTVTVSSCD730021 VL >SEQ ID NO: 7QSVLTQPPSASGTPGQRVTISCSGSRPNIGGNTVNWYQQLPGAAPKLLIYSNSQRPSGVPDRFSGSKYGTSASLAISGLQSDDEADYYCGTWDDSLNGPVFGRGTKLTVLCD730021 VH >SEQ ID NO: 8QVQLQESGPGLVRPSETLSLTCTVSGGSISSSSYYWAWVRQSPGKGLEWIGNIYYRGSTYYNPSLKSRVTMSVDMSKHQFSLKLSSLNAADTAVYYCASLYSGTYVFDYWGRGTLVTVSSCD730042 VL >SEQ ID NO: 9QSVLTQPASVSGSPGQSITISCAGTSSDVGGYNYVSWYQQHPGKAPKLMIYEGSKRPSGVSNRFSGSKSGNTASLTISGLQAEDEADYYCSSYTTRSTRVFGGGTKLTVLCD730042 VH >SEQ ID NO: 10GVQLVQSGGGLVQPGGSLRLSCAASGFTFSSYGMHWVRQAPGKGLEWVAVISYDGSIKYYADSVKGRFTISRDDSKNALYLQMNSLRAEDTAVYYCSTLSGSYGYFDYWGRGTLVTVSSCD730046 VL >SEQ ID NO: 11QSVLTQPPSASGTPGQRVTISCSGSSSNIGSNTVSWYQHLPGTAPQLLIYTNNHRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCAAWDDSLSGYVFGTGTKVTVLCD730046 VH >SEQ ID NO: 12QVQLVQSGGGVVQPGRSLRLSCAASGFTFSSYGMHWVRQAPGKGLEWVAVISYDGSIKYYADSVKGRFTISRDNSKNSLFLQMNSLRDDDTATYYCARGHLLRIGDIFYYSLDVWGQGTLV TVSSCD730047 VL >SEQ ID NO: 13QSVLTQPPSASGAPGQRVTISCSGSSSNIGSNTVNWYQRLPGAAPQLLIYNNDQRPSGIPDRFSGSKSGTSGSLVISGLQSEDEADYYCAAWDDSLSGNVFGTGTKVTVLCD730047 VH >SEQ ID NO: 14EVQLVQSGGGVVQPGRSLRLSCAASGFTFSSYGMHWVRQAPGKGLEWVAVISYDGSIKYYADSVKGRFAISRDNAKNTLYLQMNSLRREDTAMYYCASGLTGVAGALGVWGRGTLVTVS SCD730058 VL >SEQ ID NO: 15QSVLTQPPSVSVSPGQTATITCSGDRLRNEFVSWYQQRPGQSPVVVIYQDIYRPSGIPDRFSGSKSGNTATLTISGPQTVDEADYYCQAWDSNTVVFGGGTKLTVL CD730058 VH >SEQ ID NO: 16QLQLQESGSGLVKPSQTLSLICAVSGGSITSGGNAWNWIRQSPGAGLEWIGYIFSNGATYYNPSLESRVTISADTSKNQFSLTLTSVTAADTAVYYCARGDFWTGKGVFDPWGQGTLVTVSS10.3AA_HC >SEQ ID NO: 17EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSGGRTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVEPKSCDKTHTCPPCPAPEFEGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPREEQYNSTYRVVSVLTVLHQDWLNGKEYKCKVSNKALPASIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK 10.3Nt_HC >SEQ ID NO: 18GAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTTAGCAGCTATGCCTATAGCTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGCTATTAGTGGTAGTGGTGGTAGAACATACTACGCAGACTCCGTGAAGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCCGTGTATTACTGTGCGAGATTAGGGTATGGGCGGGTGGACGAGTGGGGCAGGGGAACCCTGGTCACCGTCTCGAGTGCGTCGACCAAGGGCCCATCCGTCTTCCCCCTGGCACCCTCCTCCAAGAGCACCTCTGGGGGCACAGCGGCCCTGGGCTGCCTGGTCAAGGACTACTTCCCCGAACCGGTGACGGTGTCcTGGAACTCAGGCGCtCTGACCAGCGGCGTGCACACCTTCCCGGCTGTCCTACAGTCCTCAGGACTCTACTCCCTCAGCAGCGTGGTGACCGTGCCCTCCAGCAGCTTGGGCACCCAGACCTACATCTGCAACGTGAATCACAAGCCCAGCAACACCAAGGTGGACAAGAGAGTTGAGCCCAAATCTTGTGACAAAACTCACACATgcCCacCGTGCCCAGCACCTGAATTCGAGGGGGGAcCGTCAGTCTTCCTCTTCCCCCCAAAACCCaaGgACACCCTCATGATCTCCCGGACCCCTGAGGTCACATGCGTGGTGGTGGACGTGAGCCACGAAGACCCTGAGGTCAAGTTCAACTGGTACGTGGACGGCGTGGAGGTGCATAATGCCAAGACAAAGCCGCGGGAGGAGCAGTACAACAGCACGTACCGTGTGGTCAGCGTCCTCACCGTCCTGCACCAGGACTGGCTGAATGGCAAGGAGTACAAGTGCAAGGTCTCCAACAAAGCCCTCCCAGCCTCCATCGAGAAAACCATCTCCAAAGCCAAAGGGCAGCCCCGAGAACCACAGGTcTACACCCTGCCCCCATCCCGGGAGGAGATGACCAAGAACCAGGTCAGCCTGACCTGCCTGGTCAAAGGCTTCTATCCCAGCGACATCGCCGTGGAGTGGGAGAGCAATGGGCAGCCGGAGAACAACTACAAGACCACGCCTCCCGTGCTGGACTCCGACGGCTCCTTCTTCCTCTATAGCAAGCTCACCGTGGACAAGAGCAGGTGGCAGCAGGGGAACGTCTTCTCATGCTCCGTGATGCATGAGGCTCTGCACAACCACTACACGCAGAAGAGCCTCTCCCTGTCTCCGGGTAAA10.3AA_LC >SEQ ID NO: 19QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLDNLRLSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVLGQPKAAPSVTLFPPSSEELQANKATLVCLISDFYPGAVTVAWKADSSPVKAGVETTTPSKQSNNKYAASSYLSLTPEQWKSHRSYSCQVTHEGSTVEKTVAPTECS 10.3Nt-LC >SEQ ID NO: 20CAGTCTGTGCTGACTCAGCCACCCTCAGCGTCTGGGACCCCCGGGCAGAGGGTCACCATCTCTTGTTCTGGAAGCCTCTCCAACATCGGAAGGAATCCTGTTAACTGGTATCAGCAGCTCCCAGGGACGGCCCCCAAACTCCTCATCTATCTTGATAATCTACGGCTAAGTGGGGTCCCTGACCGATTCTCTGGCTCCAAGTCTGGAACCTCAGCCTCCCTGGCCATCAGTGGGCTCCAGTCTGAGGATGAGGCTGATTATTACTGTGCAACATGGGATGACAGCCACCCCGGGTGGACGTTCGGCGGAGGGACCAAGCTGACCGTCCTAGGTCAGCCCAAGGCGGCGCCCTCGGTCACTCTGTTCCCGCCCTCCTCTGAGGAGCTTCAAGCCAACAAGGCCACACTGGTGTGTCTCATAAGTGACTTCTACCCGGGAGCCGTGACAGTGGCCTGGAAGGCAGATAGCAGCCCCGTCAAGGCGGGAGTGGAGACCACCACACCCTCCAAACAAAGCAACAACAAGTACGCGGCCAGCAGCTACCTGAGCCTGACGCCTGAGCAGTGGAAGTCCCACAGAAGCTACAGCTGCCAGGTCACGCATGAAGGGAGCACCGTGGAGAAGACAGTGGCCCCTACAGAATG TTCA10.3AA_VH >SEQ ID NO: 21EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSGGRTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSS10.3Nt_VH >SEQ ID NO: 22GAGGTGCAGCTGTTGGAGTCTGGGGGAGGCTTGGTACAGCCTGGGGGGTCCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTTAGCAGCTATGCCTATAGCTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCAGCTATTAGTGGTAGTGGTGGTAGAACATACTACGCAGACTCCGTGAAGGGCCGGTTCACCATCTCCAGAGACAATTCCAAGAACACGCTGTATCTGCAAATGAACAGCCTGAGAGCCGAGGACACGGCCGTGTATTACTGTGCGAGATTAGGGTATGGGCGGGTGGACGAGTGGGGCAGGGGAACCCTGGTCACCGTCTCGAGT10.3AA_VL >SEQ ID NO: 23QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLDNLRLSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVL 10.3Nt-VL >SEQ ID NO: 24CAGTCTGTGCTGACTCAGCCACCCTCAGCGTCTGGGACCCCCGGGCAGAGGGTCACCATCTCTTGTTCTGGAAGCCTCTCCAACATCGGAAGGAATCCTGTTAACTGGTATCAGCAGCTCCCAGGGACGGCCCCCAAACTCCTCATCTATCTTGATAATCTACGGCTAAGTGGGGTCCCTGACCGATTCTCTGGCTCCAAGTCTGGAACCTCAGCCTCCCTGGCCATCAGTGGGCTCCAGTCTGAGGATGAGGCTGATTATTACTGTGCAACATGGGATGACAGCCACCCCGGGTGGACGTTCGGCGGAGGGACCAAGCTGACCGTCCTACD7300010 parent FW1-VL >SEQ ID NO: 25 LPVLTQPPSVSGTPGQRVTISCCD7300010 GL FW1-VL >SEQ ID NO: 26 QSVLTQPPSASGTPGQRVTISCCD7300010 parent FW2-VL >SEQ ID NO: 27 WYKQVPGTAPKLLIYCD7300010 GL FW2-VL >SEQ ID NO: 28 WYQQLPGTAPKLLIYCD7300010 parent/GL FW3-VL >SEQ ID NO: 29GVPDRFSGSKSGTSASLAISGLQSEDEADYYCCD7300010 parent/GL FW4-VL (also CD370002 and 2C5) >SEQ ID NO: 30FGGGTKLTVLCD7300010 parent/GL FW1-VH (also CD370002 and 2C5) >SEQ ID NO: 31EVQLLESGGGLVQPGGSLRLSCAASGFTFSCD7300010 parent/GL FW2-VH (also CD370002 and 2C5) >SEQ ID NO: 32WVRQAPGKGLEWVSCD7300010 parent/GL FW3-VH (also CD370002 and 2C5) >SEQ ID NO: 33RFTISRDNSKNTLYLQMNSLRAEDTAVYYCARCD7300010 parent/GL FW4-VH >SEQ ID NO: 34 WGRGTLVTVSSCD7300010 CDR1-VH (also CD370002 and 2C5) >SEQ ID NO: 35 SYAMS10.3 CDR1-VH >SEQ ID NO: 36 SYAYS CDR2-VH (also CD370002) >SEQ ID NO: 37AISGSGGSTYYADSVKG CDR2-VH >SEQ ID NO: 38 LIWGSWGSTYYADSVKGCDR2-VH >SEQ ID NO: 39 AISGSGGRTYYADSVKG CDR2-VH >SEQ ID NO: 40AISGSWGRTYYADSVKG CDR3-VH >SEQ ID NO: 41 LGYSTIDY CDR3-VH >SEQ ID NO: 42LGYSTIDK CDR3-VH >SEQ ID NO: 43 LGYSTIDM CDR3-VH >SEQ ID NO: 44 LGYSTIDLCDR3-VH >SEQ ID NO: 45 LGYGRVDE CDR1-VL >SEQ ID NO: 46 SGSLSNIGRNPVNCDR1-VL >SEQ ID NO: 47 SGSLSNIGRNEVN CDR1-VL >SEQ ID NO: 48SGSLSNIGRNDVN CDR2-VL >SEQ ID NO: 49 LNNQRPS CDR2-VL >SEQ ID NO: 50LDNLRLG CDR2-VL >SEQ ID NO: 51 LDNLRLS CDR2-VL >SEQ ID NO: 52 LNNQRLGCDR3-VL >SEQ ID NO: 53 ATWDDSLNGWL CDR3-VL >SEQ ID NO: 54 ATWDDSLKGWLCDR3-VL >SEQ ID NO: 55 ATWDDSLIGWL CDR3-VL >SEQ ID NO: 56 ATWDDSHPGWTCD730010-VL >SEQ ID NO: 57LPVLTQPPSVSGTPGQRVTISCSGSLSNIGRNPVNWYKQVPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLNGWLFGGGTKLTVLCD730010GL9-VL >SEQ ID NO: 58QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLNGWLFGGGTKLTVL P32E-VL >SEQ ID NO: 59QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNEVNWYQQLPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLNGWLFGGGTKLTVL C1-VL >SEQ ID NO: 60QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNEVNWYQQLPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLKGWLFGGGTKLTVL C2-VL >SEQ ID NO: 61QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLDNLRLGGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLKGWLFGGGTKLTVL D3-VL >SEQ ID NO: 62QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLDNLRLSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLIGWLFGGGTKLTVL G10-VL >SEQ ID NO: 63QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNDVNWYQQLPGTAPKLLIYLNNQRLGGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLKGWLFGGGTKLTVL HPT-VL >SEQ ID NO: 64QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVL GRVE-VL >SEQ ID NO: 65QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSLNGWLFGGGTKLTVL 73combo1 (C1 + GRVE +HPT)-VL >SEQ ID NO: 66QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNEVNWYQQLPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVL 73combo2 (C2 + GRVE +HPT)-VL >SEQ ID NO: 67QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLDNLRLGGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVL 73combo3(D3 + GRVE +HPT)-VL [10.3] >SEQ ID NO: 68QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLDNLRLSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVL 73combo5 (G10 + GRVE +HPT)-VL >SEQ ID NO: 69QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNDVNWYQQLPGTAPKLLIYLNNQRLGGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVL 73combo6(GRVE +HPT)-VL >SEQ ID NO: 70QSVLTQPPSASGTPGQRVTISCSGSLSNIGRNPVNWYQQLPGTAPKLLIYLNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCATWDDSHPGWTFGGGTKLTVLCD730010-VH >SEQ ID NO: 71EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDYWGRGTLVTVSSCD730010GL9-VH >SEQ ID NO: 72EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDYWGRGTLVTVSSP32E-VH >SEQ ID NO: 73EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDYWGRGTLVTVSSC1-VH >SEQ ID NO: 74EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDKWGRGTLVTVSSC2-VH >SEQ ID NO: 75EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSLIWGSWGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDMWGRGTLVTVSSD3-VH >SEQ ID NO: 76EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSGGRTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDLWGRGTLVTVSSG10-VH >SEQ ID NO: 77EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSWGRTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDLWGRGTLVTVSSHPT-VH >SEQ ID NO: 78EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYSTIDYWGRGTLVTVSSGRVE-VH >SEQ ID NO: 79EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSS 73combo1 (C1 +GRVE + HPT)-VH >SEQ ID NO: 80EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSS 73combo2 (C2 +GRVE + HPT)-VH >SEQ ID NO: 81EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSLIWGSWGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSS 73combo3(D3 +GRVE + HPT)-VH [10.3] >SEQ ID NO: 82EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSGGRTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSS 73combo5 (G10 +GRVE + HPT)-VH >SEQ ID NO: 83EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAYSWVRQAPGKGLEWVSAISGSWGRTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSS73combo6(GRVE + HPT)-VH >SEQ ID NO: 84EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARLGYGRVDEWGRGTLVTVSSCD730002VH >SEQ ID NO: 85EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSCD730002VL >SEQ ID NO: 86QSVLTQPPSVSVSPGQTATITCSGDKVGDKYASWYQQKPGQSPVLVIYEDTKRPSRIPERFSGSNSGNTATLTISGTQALDEADYFCQAWDTSFWVFGGGTKLTVL 2C5VH >SEQ ID NO: 87EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKRRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSS2C5VL >SEQ ID NO: 88QSVLTQPPSVSVSPGQTASITCSGDKVGDKYASWYQQKPGQSPVLVIYEDTKRLSGIPERFSGSNSGNTATLTISGTQAMDEADYYCQAWDTSFWVFGGGTKLTVLCD730002 parent/2C5 FW4-VH >SEQ ID NO: 89 WGQGTMVTVSSCD730002 parent FW1-VL >SEQ ID NO: 90 QSVLTQPPSVSVSPGQTATITCCD7300002 2C5 FW1-VL >SEQ ID NO: 91 QSVLTQPPSVSVSPGQTASITCCD730002 parent/2C5 FW2-VL >SEQ ID NO: 92 WYQQKPGQSPVLVIYCD730002 parent FW3-VL >SEQ ID NO: 93 RIPERFSGSNSGNTATLTISGTQALDEADYFCCD730002/2C5 FW3-VL >SEQ ID NO: 94 GIPERFSGSNSGNTATLTISGTQAMDEADYYCCD730002/2C5 CDR2-VH >SEQ ID NO: 95 AISGSGGSTYYADSVKRCD730002 parent/2C5 CDR3-VH >SEQ ID NO: 96 DKGYYWYMDVCD730002 parent/2C5 CDR1-VL >SEQ ID NO: 97 SGDKVGDKYASCD730002 parent CDR2-VL >SEQ ID NO: 98 EDTKRPSCD730002 2C5 CDR2-VL >SEQ ID NO: 99 EDTKRLSCD730002 parent/2C5 CDR3-VL >SEQ ID NO: 100 QAWDTSFWVPhen0203-VH >SEQ ID NO: 101EVQLVQSGGGVVQPGRSLRLSCAASGFRFSDFAMHWVRQAPGKGLEWVAGISYDGGNKYYADSVKGRFTISRDNSNNTLYLQMNSLRAEDTAVYYCAKDHGYSGYYGHLDYWGRGTLV TVSSPhen0203-VL >SEQ ID NO: 102QSVVTQPPSASGTPGQRVTISCSGSSSNIGSNTVNWYQQLPGTAPKLLIYSNNQRPSGVPDRFSGSKSGTSASLAISGLQSEDEADYYCAAWDDSLNGRVFGTGTKLTVLCD730004-VH >SEQ ID NO: 103EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAKDRPNYYGASGSYYKQGGDHWGQ GTMVTVSSCD730004-VL >SEQ ID NO: 104NFMLTQPHSVSESPGQTVTISCTRSSGSIASKYVQWYQKRPGSSPTTVIYEDTQRPSGVPDRFSGSIDISSNSASLTISGLRTEDEADYYCQSYDSTNWVFGGGTKVTVLCD730008-VH >SEQ ID NO: 105EVQLLETGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARGNYGNLDHWGKGTLVTVSSCD730008-VL >SEQ ID NO: 106QSVLTQPPSVSVSPGQTASITCSGDKVGDKYASWYQQKPGQSPVLVIYQDRKRPSGIPERFSGSNSGNTATLTISGTQPMDEADYYCQAWDSSHWVFGGGTKLTVL CD730068-VH >SEQ ID NO: 107EVQLLESGGGLVQPGGSLRLSCAASGFTFSNYIMGWVRQAPGKGLEWVSSISSSGGATIYADSVKGRFTISRDNSKNTLYLQMNSLRAEDMAVYYCAKDHLGGHGMDVWGQGTTVTVSSCD730068-VL >SEQ ID NO: 108DIQMTQSPSSLSASVGDRVTITCRASQDISNYLAWFQQKPGKAPKSLIFAASSLESGVPSKFSGSGSGTDFTLTISSLQPEDSATYYCQQYNSYPLTFGGGTKVEIK CD730069-VH >SEQ ID NO: 109EVQLLESGGGLVQPGGSLRLSCAASGFTFSEYQMGWVRQAPGKGLEWVSYIRSSGGQTIYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARRTYSSGWHIDYWGQGTLVTVSSCD730069-VL >SEQ ID NO: 110DIQMTQSPDSLSASVGDRVTITCRASQSISRYLNWYQQKPGKAPKLLIYGASSLQSGVPSRFSGSGSGTDFSLTISSLQLEDFATYYCQQSYRTPLTFGGGTKVEIQClone 2 SGMY-VH >SEQ ID NO: 111EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSClone 2 SGMY-VL >SEQ ID NO: 112QSVLTQPPSVSVSPGQTASITCSGDKVGDKYASWYQQKPGQSPVLVIYEDTKRPSGIPERFSGSNSGNTATLTISGTQAMDEADYYCQAWDTSFWVFGGGTKLTVLCDRH1 Y32V-VH >SEQ ID NO: 113EVQLLESGGGLVQPGGSLRLSCAASGFTFSSVAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSCDRH1 M34R-VH >SEQ ID NO: 114EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYARSWVRQAPGKGLEWVSAISGSGGSTYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSCDRH2 T57P-VH >SEQ ID NO: 115EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSPYYADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSCDRH2 A60G-VH >SEQ ID NO: 116EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYGDSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSCDRH2 G65R-VH >SEQ ID NO: 117EVQLLESGGGLVQPGGSLRLSCAASGFTFSSYAMSWVRQAPGKGLEWVSAISGSGGSTYYADSVKRRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARDKGYYWYMDVWGQGTMVTVSSCDRL2 T52S-VL >SEQ ID NO: 118QSVLTQPPSVSVSPGQTASITCSGDKVGDKYASWYQQKPGQSPVLVIYEDSKRPSGIPERFSGSNSGNTATLTISGTQAMDEADYYCQAWDTSFWVFGGGTKLTVLLCDRL2 R54Y-VL >SEQ ID NO: 119QSVLTQPPSVSVSPGQTASITCSGDKVGDKYASWYQQKPGQSPVLVIYEDTKYPSGIPERFSGSNSGNTATLTISGTQAMDEADYYCQAWDTSFWVFGGGTKLTVLVLCDRL2 P55H-VL >SEQ ID NO: 120QSVLTQPPSVSVSPGQTASITCSGDKVGDKYASWYQQKPGQSVLVIYEDTKRHSGIPERFSGSNSGNTATLTISGTQAMDEADYYCQAWDTSFWVFGGGTKLTVLVLCDRL2 P55L-VL >SEQ ID NO: 121QSVLTQPPSVSVSPGQTASITCSGDKVGDKYASWYQQKPGQSPVLVIYEDTKRLSGIPERFSGSNRGNTATLTISGTQAMDEADYYCQAWDTSFWVFGGGTKLTVLVL2SGMY FW3-VL >SEQ ID NO: 122 GIPERFSGSNRGNTATLTISGTQAMDEADYYCCDRH1 Y32V CDR1-VH >SEQ ID NO: 123 SVAMSCDRH1 M34R CDR1-VH >SEQ ID NO: 124 SYARSCDRH2 T57P CDR2-VH >SEQ ID NO: 125 AISGSGGSPYYADSVKGCDRH2 A60G CDR2-VH >SEQ ID NO: 126 AISGSGGSTYYGDSVKGCDRL2 T52S CDR2-VL >SEQ ID NO: 127 EDSKRPSCDRL2 R54H CDR2-VL >SEQ ID NO: 128 EDTKYPSCDRL2 P55H CDR2-VL >SEQ ID NO: 129 EDTKRLS

What is claimed is:
 1. A method of inhibiting tumor growth in a subjectcomprising administering an anti-CD73 antibody, or an antigen-bindingfragment thereof, and an A2A receptor inhibitor for inhibiting tumorgrowth to the subject.
 2. A method of increasing an anti-tumor immuneresponse comprising administering an anti-CD73 antibody, or anantigen-binding fragment thereof, and an A2A receptor inhibitor to asubject in need thereof.
 3. A method of treating a tumor in a subjectcomprising administering an anti-CD73 antibody, or an antigen-bindingfragment thereof, and an A2A receptor inhibitor for treating a tumor toa subject.
 4. The method any one of claims 1-3, wherein the anti-CD73antibody is MEDI9447 or an antigen-binding fragment thereof.
 5. Themethod of any one of claims 1-3, wherein the anti-CD73 antibody isPhen0203 hIgG1 or an antigen-binding fragment thereof.
 6. The method ofany one of claims 1-3, wherein the A2A receptor inhibitor is SCH58261.7. The method of any one of claims 1-3, wherein the anti-CD73 antibodyis MEDI9447 or an antigen-binding fragment thereof and the A2A receptorinhibitor is SCH58261.
 8. The method of any one of claims 1-3, whereinthe anti-CD73 antibody is Phen0203 hIgG1 or an antigen-binding fragmentthereof and the A2A receptor inhibitor is SCH58261.
 9. The method of anyone of claims 1-3, wherein the anti-CD73 antibody or antigen-bindingfragment thereof and the adenosine receptor inhibitor (A2ARi) areadministered concurrently.
 10. The method of any one of claims 1-3,wherein the anti-CD73 antibody or antigen-binding fragment thereof isadministered prior to the adenosine receptor inhibitor (A2ARi).
 11. Themethod of any one of claims 1-3, wherein the adenosine receptorinhibitor (A2ARi) is administered prior to the anti-CD73 antibody orantigen-binding fragment thereof.
 12. The method of any one of claims1-3, wherein the tumor is a breast cancer, hormonally mediated breastcancer, triple negative breast cancer, colon carcinoma, colorectalcancer, lung cancer, melanoma, non-small cell carcinoma, lymphoma,Hodgkin's and non-Hodgkin's lymphoma, Burkitt's lymphoma, and sarcoma.13. The method of any one of claims 1-3, wherein said method results inan increase in overall survival as compared to the administration of anyone of the anti-CD73 antibody or the A2A receptor inhibitor alone. 14.The method of any one of claims 1-3, wherein the said method induces orincreases a tumor-specific immune response.
 15. The method of any one ofclaims 1-3, wherein the said method reduces the immunosuppressiveeffects of a AMP/CD73/adenosine pathway.
 16. The method of any one ofclaims 1-3, wherein the said method reduces metastasis or reduces thepropensity of the tumor to metastasize relative to the administration ofeither the anti-CD73 antibody or the adenosine receptor inhibitor(A2ARi) alone.
 17. The method of any one of claims 1-3, wherein the saidmethod reduces the number of metastases within the subject.
 18. Themethod of any one of claims 1-3, wherein the subject is a human patient.19. The method of any one of claims 1-3, wherein the tumor is a CD73overexpres sing tumor.
 20. The method of any one of claims 1-3, whereinthe cancer has a prometastatic phenotype.
 21. A kit for increasinganti-tumor activity, the kit comprising an anti-CD73 antibody orantigen-binding fragment thereof and an A2A receptor inhibitor.
 22. Thekit of claim 21, wherein the anti-CD73 antibody is MEDI9447 or anantigen-binding fragment thereof.
 23. The kit of claim 21, wherein theanti-CD73 antibody is Phen0203 hIgG1 or an antigen-binding fragmentthereof.
 24. The kit of claim 21, wherein the A2A receptor inhibitor isSCH58261.
 25. The kit of claim 21, wherein the anti-CD73 antibody isMEDI9447 or an antigen-binding fragment thereof and the A2A receptorinhibitor is SCH58261.
 26. The kit of claim 21, wherein the anti-CD73antibody is Phen0203 hIgG1 or an antigen-binding fragment thereof andthe A2A receptor inhibitor is SCH58261.
 27. A pharmaceutical formulationcomprising an effective amount an anti-CD73 antibody or antigen-bindingfragment thereof and an A2A receptor inhibitor.
 28. The pharmaceuticalformulation of claim 27, wherein the anti-CD73 antibody is MEDI9447 oran antigen-binding fragment thereof.
 29. The pharmaceutical formulationof claim 27, wherein the anti-CD73 antibody is Phen0203 hIgG1 or anantigen-binding fragment thereof.
 30. The pharmaceutical formulation ofclaim 27, wherein the A2A receptor inhibitor is SCH58261.
 31. Thepharmaceutical formulation of claim 27, wherein the anti-CD73 antibodyis MEDI9447 or an antigen-binding fragment thereof and the A2A receptorinhibitor is SCH58261.
 32. The pharmaceutical formulation of claim 27,wherein the anti-CD73 antibody is Phen0203 hIgG1 or an antigen-bindingfragment thereof and the A2A receptor inhibitor is SCH58261.